Chemistry. 2014 2015 Catalog. www.cengageasia.com. Chemistry 2014 2015 Catalog

Chemistry 2014 2015 Catalog Chemistry 2014 2015 Catalog CLA DEC 2013 Cengage Learning Asia Pte Ltd 151 Lorong Chuan #02-08 New Tech Park (Lobby H) Singapore 556741 Tel (65) 6410 1200 Fax (65) 6410 1208 e-mail asia.info@cengage.com

Cengage Learning Asia introducing the new... Cengage Technology Editions are being launched to support educators and learners in making a smooth transition from print to digital learning and instruction. These hybrid editions combine full ebooks or digital solutions packages with print editions for maximum flexibility and benefits, including: integrated print and digital learning media enhanced student-teacher interactions engaged students, improved learning experiences and better outcomes a growing and interconnected pool of best-selling titles from Cengage Learning Cengage Technology Editions offer the best in print and digital content to create the kinds of blended learning experiences that are fast gaining popularity among students. These editions provide hybrid alternatives to best-selling titles from Cengage Learning in disciplines such as Business and Economics, Science and Mathematics, Social Sciences and Humanities, and more. Engage with Us! Email asia.info@cengage.com

Contents Chemistry Allied Health Chemistry... 2 Analytical Chemistry... 23 Biochemistry... 27 General Chemistry...30 Inorganic Chemistry...61 Introductory / Preparatory Chemistry...62 Liberal Arts Chemistry...81 Organic Chemistry... 83 Physical Chemistry...111 Spectroscopy...114 Combined Author/Title Index...116 Order form/pricelist is available upon request through Cengage Learning Representative. Special price requests for class adoption are subject to approval. Please contact your Cengage Learning Representative for details. Information contained in this catalog is correct at the time of printing. Prices are subject to change without prior notice.

Chemistry Allied Health Chemistry Properties (Acetylsalicylic Acid). 10. Carbohydrates. 11. Fats and Oils: Preparation and Properties of Soap. 12. Acid-Base Properties of Amino Acids. 13. Isolation and Identification of Casein. 14. Enzymes. 2012, 256pp, Paperback, 9781111426613 BASIC LABORATORY EXPERIMENTS FOR GENERAL, ORGANIC, AND BIOCHEMISTRY Joseph M. Landesberg, Adelphi University Succeed in your GOB Lab course with the easy-tofollow experiments in this streamlined and focused manual. Fourteen experiments (6 general chemistry, 4 organic chemistry, and 4 biochemistry) illustrate the concepts you must know for your future allied health career, while pre- and post-lab questions test your ability to apply concepts. DESIGNED FOR NURSING AND HEALTH SCIENCE MAJORS. Focusing on the key concepts most important to allied health majors, this streamlined lab manual is ideal for the one-term General, Organic, and Biochemistry laboratory course. CLEAR AND STRAIGHTFORWARD. Clear directions help students complete labs successfully. A FOCUS ON APPLICATION. Pre- and post-lab questions for every experiment test the student s ability to understand and apply concepts. 1. Laboratory Measurements. 2. Density Determination. 3. Classes of Chemical Reactions. 4. Separation of Components of a Mixture. 5. Factors Affecting Rate of Reactions. 6. The Law of Chemical Equilibrium and the Le Chatelier Principle. 7. ph and Buffer Solutions. 8. Structure and Stereochemistry in Organic Compounds, the Use of Molecular Models. 9. Aspirin: Preparation and GENERAL, ORGANIC, AND BIOCHEMISTRY An Applied Approach, International Edition James Armstrong, City College of San Francisco Focusing on the needs of allied health and nursing majors, this engaging book is ideal for students who have had no prior exposure to chemistry. The author takes the time to explain how to do tasks that students find difficult, rather than just providing terse descriptions. Emphasizing problem-solving techniques without skipping steps and using terms students can grasp, the book takes the most direct path to biomolecules and metabolic processes, provides a wealth of worked examples to help students understand key chemical concepts, includes novel and relevant Health Notes in the margins, and weaves biological and medical applications throughout. DESIGNED FOR NURSING AND HEALTH SCIENCES MAJORS. This allied health-focused book takes the most direct path to biomolecules and metabolic processes, includes novel and relevant Health Notes in the margins, and weaves biological and medical applications throughout to prepare students for their future careers. EMPHASIS ON PROBLEM SOLVING STRATEGIES. Each Sample Problem is paired with a closely related Try It Yourself question. Most sample problems list additional Core Problems that students can do to 2

practice new skills. Steps for solving the conversion problems appear in the margins to guide students through the problem-solving process. FOCUSED ON STUDENT LEARNING. Each chapter begins with a short health-related, story type introduction, followed by numbered sections with learning objectives. Section-ending Core Problems immediately reinforce the section objectives and help students gauge their knowledge of the content. Key Terms appear in boldface type the first time they are used and are collected at the back of the chapter to facilitate student review. BUILT-IN STUDY GUIDE. End-of-chapter material (keyed to each section) helps students master chapter concepts and problem-solving skills and review for quizzes and tests. Concept Questions encourage students to describe how the ideas in the chapter apply to specific examples, while Summary and Challenge Problems cover all sections and give instructors the opportunity to assign questions at a wide range of levels. Challenge problems are marked with an asterisk and require a greater depth of understanding; many involve concepts from earlier chapters. OWL INTEGRATION. Improve student learning outcomes with OWL, the #1 online homework and learning system for chemistry. Developed by chemistry instructors for teaching chemistry, OWL includes course management tools that make homework management a breeze, as well as advanced reporting and grade book features that save time in grading homework and tracking student progress. OWL enables you to address students different learning styles through tutorials, simulations, visualization exercises, and algorithmically-generated homework questions with answer-specific feedback. With OWL s mastery learning approach, students work at their own pace until they understand each concept/skill. OWL includes an ebook, enhanced with multimedia learning tools. EXPERT REVIEW: The entire text was reviewed by Nursing Professor Kellee Hollyman, RN,BSN, MN- Nurse Educator to ensure the relevance and accuracy of the health material. 1. MEASUREMENTS IN SCIENCE AND MEDICINE. Measuring Size: Distance, Mass, and Volume. Metric Units and Their Relationships. Rounding and Precision In Measurements. Unit Conversions and Conversion Factors. Rounding and Significant Figures. Temperature. Density, Dosage, and Other Compound Units. 2. ATOMS, ELEMENTS, AND COMPOUNDS. Classifying Matter: Mixtures, Compounds, and Elements. The Chemical Elements: An Introduction to the Periodic Table. Atoms. Subatomic Particles and Atomic Structure. Isotopes And Atomic Weight. Chemical Formulas. Electron Shells. Chemical Behavior, Valence Electrons, and the Periodic Law. The Organization of the Periodic Table. 3. CHEMICAL BONDS. Covalent Bonds and the Octet Rule. Double And Triple Bonds. Drawing Lewis Structures for Complex Molecules. Electronegativity and Polar Bonds. Naming Covalent Compounds. Ions and Ionic Compounds. Writing Formulas for Ionic Compounds. Naming Ionic Compounds. Polyatomic Ions. Recognizing Ionic and Molecular Compounds. 4. ENERGY AND THE PHYSICAL BEHAVIOR OF CHEMICAL SUBSTANCES. Heat and Energy. The Three States of Matter. The Properties of Gases. Changes of State. Attractive Forces and the Physical Properties of Matter. 5. SOLUTIONS AND CONCENTRATION. Solutions and the Dissolving Process. Electrolytes and Dissociation. Solubility. The Relationship Between Solubility and Molecular Structure. Concentration. Moles and Formula Weights. Molarity. Osmosis, Dialysis, And Tonicity. Equivalents. Dilution. 6. CHEMICAL REACTIONS. Physical Changes and Chemical Reactions. Chemical Equations. Mass Relationships in a Chemical Reaction. Heats of Reaction. Combustion and Precipitation Reactions. Reaction Rate and Activation Energy. Chemical Equilibrium. 7. ACIDS AND BASES. The Self-Ionization of Water. The Ph Scale. The Properties of Acids. The Properties of Bases. Acid-Base Reactions. Amphiprotic Molecules and Ions. Buffers.The Role of Buffers in Human Physiology. 8. HYDROCARBONS AN INTRODUCTION TO ORGANIC MOLECULES. The Special Properties of Carbon. Linear Alkanes: The Foundation of Organic Chemistry. Branched Alkanes, Cycloalkanes, and Isomers. Naming Branched Alkanes: The IUPAC System. Functional Groups. Alkenes and Alkynes. Geometric Isomers. Benzene and Aromatic Compounds. The Properties of Hydrocarbons. 9. HYDRATION, DEHYDRATION AND ALCOHOLS. The Hydration Reaction. Controlling the Product An Introduction to Enzymes. Naming Alcohols. The Physical Properties 3

of Alcohols. The Dehydration Reaction. Phenols and Thiols. 10. CARBONYL COMPOUNDS AND REDOX REACTIONS. Hydrogenation and Dehydrogenation. Oxidation and Reductions. Reactions and the Carbonyl Group. The Naming and Properties of Aldehydes and Ketones. Other Oxidation and Reduction Reactions. Carboxylic Acids. Biological Oxidations and Reductions The Redox Coenzymes. Introduction to Metabolic Pathways. 11. ORGANIC ACIDS AND BASES. Reactions of Organic Acids. Decarboxylation Reactions. Amines. The Acid-Base Reactions of Amines. Amines in Biology and Medicine. The Relationship Between Structure and Ph. 12. BUILDING LARGE MOLECULES CONDENSATION AND HYDROLYSIS REACTIONS. Introduction to Condensation Reactions Ethers. Esterification, Amidation, and Phosphorylation. Condensation Polymers. Hydrolysis. The Effect of Ph on the Products of Hydrolysis. The Equilibrium Between Condensation and Hydrolysis. 13. PROTEINS. Amino acids. Peptide bonds and the secondary structure of a protein. Side chain interactions and tertiary structure. Protein denaturation. Enzyme structure and function. Cofactors. Antibodies and the immune response. Sources of amino acids. 14: CARBOHYDRATES AND LIPIDS. Monosaccharides. Isomeric Forms Of Monosaccharides Anomers and Enantiomers. Disaccharides and the Glycosidic Linkage. Common Disaccharides and Polysaccharides. Fatty Acids and Triglycerides. The Chemical Reactions of Triglycerides. Glycerophospholipids and Cell Membranes. Steroids and Lipoproteins. Sources of Carbohydrates and Fats. 15. METABOLISM THE CHEMICAL WEB OF LIFE. Catabolism, Anabolism, and the ATP Cycle. An Overview of Catabolism. ATP Production and the Mitochondria. Glycolysis. The Citric Acid Cycle. Beta Oxidation Obtaining Energy from Fatty Acids. Catabolism of Amino Acids. Anabolic Pathways and the Control of Metabolism. 16. NUCLEIC ACIDS, PROTEIN SYNTHESIS, AND HEREDITY. Nucleotides. The Structure of Nucleic Acids. DNA Replication. Transcription and RNA Processing. Translation and The Genetic Code. The Mechanism of Protein Synthesis. Regulation of Protein Synthesis. Mutations and Genetic Disorders. 17. NUCLEAR CHEMISTRY. Symbols for Nuclei And Subatomic Particles. Writing Nuclear Equations. Energy and Nuclear Reactions. Physiological Effects of Ionizing Radiation. Measuring Radiation. Nuclear Decay and Half-Life. Medical Applications of Nuclear Radiation. Nuclear Fission and Fusion. APPENDIX A: ESSENTIAL MATHEMATICS FOR CHEMISTRY. Decimal Notation. Place Value, Fractions, and Division. Order of Operations. Exponents. Scientific Notation. Calculator Use. APPENDIX B: THE QUANTITATIVE BEHAVIOR OF GASES. (Kelvin temperature, combined gas law, Avogadro s law, ideal gas law). 2012, 832pp, Paperback, 9780840068286 GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, INTERNATIONAL EDITION, 6E H. Stephen Stoker, Weber State University Emphasizing the applications of chemistry and minimizing complicated mathematics, GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, 6E, International Edition is written throughout to help students succeed in the course and master the biochemistry content so important to their future careers. The Sixth Edition s clear explanations, visual support, and effective pedagogy combine to make the text ideal for allied health majors. Early chapters focus on fundamental chemical principles while later chapters build on the foundations of these principles. Mathematics is introduced at point-of-use and only as needed. NEW TO THIS EDITION Several new Chemistry At-A-Glance boxes covering critical chemistry concepts have been added to this edition. New Chemical Connection Boxes covering a variety of topics that relate chemistry to our everyday lives!. Heavily revised art and photography program. Talking labels have been added to many of the illustrations 4

these labels help students understand the concepts being discussed in the figure. New questions and problems have been added to the end of chapter question/problem sets including a new type of problem that is related to the Chemical Connection boxes the new questions are identified with an icon. Up to date coverage throughout the text, but especially the biochemistry chapters. Biochemistry is an ever changing field and the new edition has been updated with the latest information in that field. OWL and Youbook: OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. Also includes Student Self Assessments, the interactive customizable Cengage YouBook, and an optional Solutions Manual ebook. Chemistry at-a-glance features provide brief visual summaries of core chapter concepts to help students visualize difficult material. Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students future careers in the health and environmental fields. Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students future careers in the health and environmental fields. Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students future careers in the health and environmental fields. PART I: GENERAL CHEMISTRY. 1. Basic Concepts About Matter. Chemistry: The Study of Matter. Physical States of Matter. Properties of Matter. Changes in Matter. CHEMISTRY AT A GLANCE: Use of the Terms Physical and Chemical. Pure Substances and Mixtures. Elements and Compounds. CHEMISTRY AT A GLANCE: Classes of Matter. Discovery and Abundance of the Elements. Names and Chemical Symbols of the Elements. Atoms and Molecules. Chemical Formulas. CHEMICAL CONNECTIONS: Good Versus Bad Properties for a Chemical Substance Elemental Composition of the Human Body. 2. Measurements in Chemistry. Measurement Systems. Metric System Units. Exact and Inexact Numbers. Uncertainty in Measurement and Significant Figures. CHEMISTRY AT A GLANCE: Significant Figures. Significant Figures and Mathematical Operations. Scientific Notation. Conversion Factors. Dimensional Analysis. CHEMISTRY AT A GLANCE: Conversion Factors. Density. Temperature Scales. Heat Energy and Specific Heat. CHEMICAL CONNECTIONS: Body Density and Percent Body Fat; Normal Human Body Temperature. 3. Atomic Structure and the Periodic Table. Internal Structure of an Atom. Atomic Number and Mass Number. Isotopes and Atomic Masses. CHEMISTRY AT A GLANCE: Atomic Structure. The Periodic Law and the Periodic Table. Metals and Nonmetals. Electron Arrangements Within Atoms. CHEMISTRY AT A GLANCE: Shell Subshell Orbital Interrelationships. Electron Configurations and Orbital Diagrams. The Electronic Basis for the Periodic Law and the Periodic Table. Classification of the Elements. CHEMISTRY AT A GLANCE: Element Classification Schemes and the Periodic Table. CHEMICAL CONNECTIONS: Protium, Deuterium, and Tritium: The Three Isotopes of Hydrogen; Metallic Elements and the Human Body; Iron: The Most Abundant Transition Element in the Human Body. 4. Chemical Bonding: The Ionic Bond Model. Chemical Bonds. Valence Electrons and Lewis Symbols. The Octet Rule. The Ionic Bond Model. The Sign and Magnitude of Ionic Charge. Lewis Structures for Ionic Compounds. Chemical Formulas for Ionic Compounds. The Structure of Ionic Compounds. Recognizing and Naming Binary Ionic Compounds. CHEMISTRY AT A GLANCE: Ionic Bonds and Ionic Compounds. Polyatomic Ions Chemical Formulas and Names for Ionic Compounds Containing Polyatomic Ions. CHEMISTRY AT A GLANCE: Nomenclature of Ionic Compounds. CHEMICAL CONNECTIONS: Fresh Water, Seawater, Hard Water, and Soft Water: A Matter of Ions; Tooth Enamel: A Combination of Monatomic and Polyatomic Ions. 5. Chemical Bonding: The Covalent Bond Model. The Covalent Bond Model. Lewis Structures for Molecular Compounds. Single, Double, and Triple Covalent Bonds. Valence Electrons and Number of Covalent Bonds Formed. Coordinate Covalent Bonds. Systematic Procedures for Drawing Lewis Structures. Bonding in Compounds with 5

Polyatomic Ions Present. Molecular Geometry. CHEMISTRY AT A GLANCE: The Geometry of Molecules. Electronegativity. Bond Polarity. Molecular Polarity. CHEMISTRY AT A GLANCE: Covalent Bonds and Molecular Compounds. Naming Binary Molecular Compounds. CHEMICAL CONNECTIONS: Nitric Oxide: A Molecule Whose Bonding Does Not Follow The Rules ; The Chemical Senses of Smell and Taste. 6. Chemical Calculations: Formula Masses, Moles, and Chemical Equations. Formula Masses. The Mole: A Counting Unit for Chemists. The Mass of a Mole. Chemical Formulas and the Mole Concept. The Mole and Chemical Calculations. Writing and Balancing Chemical Equations. Chemical Equations and the Mole Concept. CHEMISTRY AT A GLANCE: Relationships Involving the Mole Concept. Chemical Calculations Using Chemical Equations. CHEMICAL CONNECTIONS: Carbon Monoxide Air Pollution: A Case of Combining Ratios Chemical Reactions on an Industrial Scale: Sulfuric Acid. 7. Gases, Liquids, and Solids. The Kinetic Molecular Theory of Matter. Kinetic Molecular Theory and Physical States. Gas Law Variables. Boyle s Law: A Pressure-Volume Relationship. Charles s Law: A Temperature-Volume Relationship. The Combined Gas Law. The Ideal Gas Law. Dalton s Law of Partial Pressures. CHEMISTRY AT A GLANCE: The Gas Laws. Changes of State. Evaporation of Liquids. Vapor Pressure of Liquids. Boiling and Boiling Point. Intermolecular Forces in Liquids. CHEMISTRY AT A GLANCE: Intermolecular Forces. CHEMICAL CONNECTIONS: The Importance of Gas Densities; Blood Pressure and the Sodium Ion/ Potassium Ion Ratio; Hydrogen Bonding and the Density of Water. 8. Solutions. Characteristics of Solutions. Solubility. Solution Formation. Solubility Rules. Solution Concentration Units. Dilution. CHEMISTRY AT A GLANCE: Solutions. Colloidal Dispersions and Suspensions. Colligative Properties of Solutions. Osmosis and Osmotic Pressure. CHEMISTRY AT A GLANCE: Summary of Colligative Property Terminology. Dialysis. CHEMICAL CONNECTIONS: Factors Affecting Gas Solubility; Solubility of Vitamins; Controlled- Release Drugs: Regulating Concentration, Rate, and Location of Release; The Artificial Kidney: A Hemodialysis Machine. 9. Chemical Reactions. Types of Chemical Reactions. Redox and Nonredox Chemical Reactions. CHEMISTRY AT A GLANCE: Types of Chemical Reactions. Terminology Associated with Redox Processes. Collision Theory and Chemical Reactions. Exothermic and Endothermic Chemical Reactions. Factors That Influence Chemical Reaction Rates. Chemical Equilibrium. CHEMISTRY AT A GLANCE: Factors That Increase Reaction Rates. Equilibrium Constants. Altering Equilibrium Conditions: Le Châtelier s Principle. CHEMICAL CONNECTIONS: Combustion Reactions, Carbon Dioxide, and Global Warming; Undesirable Oxidation Reduction Processes: Metallic Corrosion; Stratospheric Ozone: An Equilibrium Situation. 10. Acids, Bases, and Salts. Arrhenius Acid Base Theory. Brønsted Lowry Acid Base Theory. Mono-, Di-, and Triprotic Acids. CHEMISTRY AT A GLANCE: Acid Base Definitions. Strengths of Acids and Bases. Ionization Constants for Acids and Bases. Salts. Acid Base Neutralization Chemical Reactions. Self-Ionization of Water. The ph Concept. The pka Method for Expressing Acid Strength. The ph of Aqueous Salt Solutions. CHEMISTRY AT A GLANCE: Acids and Acidic Solutions. Buffers. The Henderson Hasselbalch Equation. CHEMISTRY AT A GLANCE: Buffer Systems. Electrolytes. Equivalents and Milliequivalents of Electrolytes. Acid Base Titrations. CHEMICAL CONNECTIONS: Excessive Acidity Within the Stomach: Antacids and Acid Inhibitors; Acid Rain: Excess Acidity; Blood Plasma ph and Hydrolysis; Buffering Action in Human Blood; Electrolytes and Body Fluids. 11. Nuclear Chemistry. Stable and Unstable Nuclides. The Nature of Radioactive Emissions. Equations for Radioactive Decay. Rate of Radioactive Decay. CHEMISTRY AT A GLANCE: Radioactive Decay. Transmutation and Bombardment Reactions. Radioactive Decay Series. Chemical Effects of Radiation. Biochemical Effects of Radiation. Detection of Radiation. Sources of Radiation Exposure. Nuclear Medicine. Nuclear Fission and Nuclear Fusion. CHEMISTRY AT A GLANCE: Characteristics of Nuclear Reactions. Nuclear and Chemical Reactions Compared. CHEMICAL CONNECTIONS: Tobacco Radioactivity and the Uranium-238 Decay Series; Preserving Food Through Food Irradiation; The Indoor Radon-222 Problem. PART II: ORGANIC CHEMISTRY. 12. Saturated Hydrocarbons. Organic and Inorganic Compounds. Bonding Characteristics of the Carbon Atom. Hydrocarbons and Hydrocarbon Derivatives. Alkanes: Acyclic Saturated Hydrocarbons. Structural Formulas. Alkane Isomerism. Conformations of Alkanes. IUPAC Nomenclature for 6

Alkanes. Line-Angle Structural Formulas for Alkanes. CHEMISTRY AT A GLANCE: Structural Representations for Alkane Molecules. Classification of Carbon Atoms. Branched-Chain Alkyl Groups. Cycloalkanes. IUPAC Nomenclature for Cycloalkanes. Isomerism in Cycloalkanes. Sources of Alkanes and Cycloalkanes. Physical Properties of Alkanes and Cycloalkanes. Chemical Properties of Alkanes and Cycloalkanes. CHEMISTRY AT A GLANCE: Properties of Alkanes and Cycloalkanes. Nomenclature and Properties of Halogenated Alkanes. CHEMICAL CONNECTIONS: The Occurrence of Methane; The Physiological Effects of Alkanes; Chlorofluorocarbons and the Ozone Layer. 13. Unsaturated Hydrocarbons. Unsaturated Hydrocarbons. Characteristics of Alkenes and Cycloalkenes. IUPAC Nomenclature for Alkenes and Cycloalkenes. Line-Angle Structural Formulas for Alkenes. Constitutional Isomerism in Alkenes. Cis Trans Isomerism in Alkenes. Naturally Occurring Alkenes. Physical Properties of Alkenes and Cycloalkenes. Chemical Reactions of Alkenes. Polymerization of Alkenes: Addition Polymers. Alkynes. CHEMISTRY AT A GLANCE: Chemical Reactions of Alkenes 383. CHEMISTRY AT A GLANCE: IUPAC Nomenclature for Alkanes, Alkenes, and Alkynes. Aromatic Hydrocarbons. Names for Aromatic Hydrocarbons. Aromatic Hydrocarbons: Physical Properties and Sources. Chemical Reactions of Aromatic Hydrocarbons. Fused-Ring Aromatic Hydrocarbons. CHEMICAL CONNECTIONS: Ethene: A Plant Hormone and High-Volume Industrial Chemical; Cis Trans Isomerism and Vision; Carotenoids: A Source of Color; Fused-Ring Aromatic Hydrocarbons and Cancer. 14. Alcohols, Phenols, and Ethers. Bonding Characteristics of Oxygen Atoms in Organic Compounds. Structural Characteristics of Alcohols. Nomenclature for Alcohols. Isomerism for Alcohols. Important Commonly Encountered Alcohols. Physical Properties of Alcohols. Preparation of Alcohols. Classification of Alcohols. Chemical Reactions of Alcohols. CHEMISTRY AT A GLANCE: Summary of Chemical Reactions Involving Alcohols. Polymeric Alcohols. Structural Characteristics of Phenols. Nomenclature for Phenols. Physical and Chemical Properties of Phenols. Occurrence of and Uses for Phenols. Structural Characteristics of Ethers. Nomenclature for Ethers. Isomerism for Ethers. Physical and Chemical Properties of Ethers. Cyclic Ethers. Sulfur Analogs of Alcohols. Sulfur Analogs of Ethers. CHEMICAL CONNECTIONS: Menthol: A Useful Naturally Occurring Terpene Alcohol; Ethers as General Anesthetics; Marijuana: The Most Commonly Used Illicit Drug; Garlic and Onions: Odiferous Medicinal Plants. CHEMISTRY AT A GLANCE: Alcohols, Thiols, Ethers, and Thioethers. 15. Aldehydes and Ketones. The Carbonyl Group. Compounds Containing a Carbonyl Group. The Aldehyde and Ketone Functional Groups. Nomenclature for Aldehydes. Nomenclature for Ketones. Isomerism for Aldehydes and Ketones. Selected Common Aldehydes and Ketones. Physical Properties of Aldehydes and Ketones. Preparation of Aldehydes and Ketones. Oxidation and Reduction of Aldehydes and Ketones. Reaction of Aldehydes and Ketones with Alcohols. CHEMISTRY AT A GLANCE: Summary of Chemical Reactions Involving Aldehydes and Ketones. Formaldehyde-Based Polymers. Sulfur-Containing Carbonyl Groups. CHEMICAL CONNECTIONS: Lachrymatory Aldehydes and Ketones; Melanin: A Hair and Skin Pigment; Diabetes, Aldehyde Oxidation, and Glucose Testing. 16. Carboxylic Acids, Esters, and Other Acid Derivatives. Structure of Carboxylic Acids and Their Derivatives. IUPAC Nomenclature for Carboxylic Acids. Common Names for Carboxylic Acids. Polyfunctional Carboxylic Acids. Metabolic Acids. Physical Properties of Carboxylic Acids. Preparation of Carboxylic Acids. Acidity of Carboxylic Acids. Carboxylic Acid Salts. Structure of Esters. Preparation of Esters. CHEMISTRY AT A GLANCE: Summary of the H Versus R Relationship for Pairs of Hydrocarbon Derivatives. Nomenclature for Esters. Selected Common Esters. Isomerism for Carboxylic Acids and Esters. Physical Properties of Esters. Chemical Reactions of Esters. Sulfur Analogs of Esters. CHEMISTRY AT A GLANCE: Summary of Chemical Reactions Involving Carboxylic Acids and Esters. Polyesters. Acid Chlorides and Acid Anhydrides. Esters and Anhydrides of Inorganic Acids. CHEMICAL CONNECTIONS: Nonprescription Pain Relievers Derived from Propanoic Acid Carboxylic Acids and Skin Care; Aspirin; Nitroglycerin: An Inorganic Triester. 17. Amines and Amides. Bonding Characteristics of Nitrogen Atoms in Organic Compounds. Structure and Classification of Amines. Nomenclature for Amines. Isomerism for Amines. Physical Properties of Amines. Basicity of Amines. Amine Salts. Preparation of Amines and Quaternary Ammonium Salts. Heterocyclic Amines. Selected Biochemically Important Amines. Alkaloids. 7

Structure and Classification of Amides. Nomenclature for Amides. Selected Amides and Their Uses. Physical Properties of Amides. Preparation of Amides. Hydrolysis of Amides.Polyamides and Polyurethanes. CHEMISTRY AT A GLANCE: Summary of Chemical Reactions Involving Amines and Amides. CHEMICAL CONNECTIONS: Caffeine: The Most Widely Used Central Nervous System Stimulant; Nicotine Addiction: A Widespread Example of Drug Dependence; Alkaloids Present in Chocolate; Acetaminophen: A Substituted Amide. PART III: BIOLOGICAL CHEMISTRY. 18. Carbohydrates. Biochemistry An Overview. Occurrence and Functions of Carbohydrates. Classification of Carbohydrates. Chirality: Handedness in Molecules. Stereoisomerism: Enantiomers and Diastereomers. Designating Handedness Using Fischer Projection Formulas. CHEMISTRY AT A GLANCE: Constitutional Isomers and Stereoisomers. Properties of Enantiomers. Classification of Monosaccharides. Biochemically Important Monosaccharides. Cyclic Forms of Monosaccharides. Haworth Projection Formulas. Reactions of Monosaccharides. Disaccharides. CHEMISTRY AT A GLANCE: Sugar Terminology Associated with Monosaccharides and Their Derivatives. General Characteristics of Polysaccharides. Storage Polysaccharides. Structural Polysaccharides. CHEMISTRY AT A GLANCE: Types of Glycosidic Linkages for Common Glucose-Containing Diand Polysaccharides. Acidic Polysaccharides. Glycolipids and Glycoproteins: Cell Recognition. Dietary Considerations and Carbohydrates. CHEMICAL CONNECTIONS: Blood Types and Monosaccharides; Lactose Intolerance and Galactosemia; Changing Sugar Patterns: Decreased Sucrose, Increased Fructose; Artificial Sweeteners; Good and Bad Carbs : The Glycemic Index. 19. Lipids. Structure and Classification of Lipids. Types of Fatty Acids. Physical Properties of Fatty Acids. Energy-Storage Lipids: Triacylglycerols. Dietary Considerations and Triacylglycerols. Chemical Reactions of Triacylglycerols. CHEMISTRY AT A GLANCE: Classification Schemes for Fatty Acid Residues Present in Triacylglycerols. Membrane Lipids: Phospholipids. Membrane Lipids: Sphingoglycolipids. CHEMISTRY AT A GLANCE: Terminology for and Structural Relationships Among Various Types of Fatty-Acid-Containing Lipids. Membrane Lipids: Cholesterol. Cell Membranes. Emulsification Lipids: Bile Acids. Messenger Lipids: Steroid Hormones. Messenger Lipids: Eicosanoids. Protective-Coating Lipids: Biological Waxes. CHEMISTRY AT A GLANCE: Types of Lipids in Terms of How They Function. CHEMICAL CONNECTIONS: The Fat Content of Tree Nuts and Peanuts; Artificial Fat Substitutes; The Cleansing Action of Soap; Trans Fatty Acids and Blood Cholesterol Levels; Steroid Drugs in Sports; The Mode of Action for Anti-Inflammatory Drugs. 20. Proteins. Characteristics of Proteins. Amino Acids: The Building Blocks for Proteins. Chirality and Amino Acids. Acid Base Properties of Amino Acids. Cysteine: A Chemically Unique Amino Acid. Peptides. Biochemically Important Small Peptides. General Structural Characteristics of Proteins. Primary Structure of Proteins. Secondary Structure of Proteins. Tertiary Structure of Proteins. Quaternary Structure of Proteins. Protein Classification Based on Shape. Protein Classification Based on Function. CHEMISTRY AT A GLANCE: Protein Structure. Protein Hydrolysis. Protein Denaturation. Glycoproteins. Lipoproteins. CHEMICAL CONNECTIONS: The Essential Amino Acids; Substitutes for Human Insulin Protein Structure and the Color of Meat; Denaturation and Human Hair; Cyclosporine: An Antirejection Drug; Lipoproteins and Heart Disease Risk. 21. Enzymes and Vitamins. General Characteristics of Enzymes. Enzyme Structure. Nomenclature and Classifi cation of Enzymes. Models of Enzyme Action. Enzyme Specificity. Factors That Affect Enzyme Activity. CHEMISTRY AT A GLANCE: Enzyme Activity. Enzyme Inhibition. CHEMISTRY AT A GLANCE: Enzyme Inhibition. Regulation of Enzyme Activity. Antibiotics That Inhibit Enzyme Activity. Medical Uses of Enzymes. General Characteristics of Vitamins. Water-Soluble Vitamins. Fat-Soluble Vitamins. CHEMICAL CONNECTIONS: H. pylori and Stomach Ulcers; Enzymatic Browning: Discoloration of Fruits and Vegetables; Heart Attacks and Enzyme Analysis. 22. Nucleic Acids. Types of Nucleic Acids. Nucleotides: Building Blocks of Nucleic Acids. Primary Nucleic Acid Structure. CHEMISTRY AT A GLANCE: Nucleic Acid Structure. The DNA Double Helix. Replication of DNA Molecules. Overview of Protein Synthesis. Ribonucleic Acids. CHEMISTRY AT A GLANCE: DNA Replication. Transcription: RNA Synthesis. The Genetic Code. Anticodons and trna Molecules. Translation: Protein Synthesis. Mutations. Nucleic Acids and Viruses. CHEMISTRY AT A GLANCE: Protein Synthesis: Transcription and Translation. Recombinant DNA and 8

Genetic Engineering. The Polymerase Chain Reaction. DNA Sequencing. CHEMICAL CONNECTIONS: Use of Synthetic Nucleic Acid Bases in Medicine; Antibiotics That Inhibit Bacterial Protein Synthesis. 23. Biochemical Energy Production. Metabolism. Metabolism and Cell Structure. Important Intermediate Compounds in Metabolic Pathways. High-Energy Phosphate Compounds. An Overview of Biochemical Energy Production. The Citric Acid Cycle. CHEMISTRY AT A GLANCE: Simplified Summary of the Four Stages of Biochemical Energy Production. CHEMISTRY AT A GLANCE: Summary of the Reactions of the Citric Acid Cycle. The Electron Transport Chain. CHEMISTRY AT A GLANCE: Summary of the Flow of Electrons Through the Four Complexes of the Electron Transport Chain. Oxidative Phosphorylation. CHEMISTRY AT A GLANCE: Summary of the Common Metabolic Pathway. ATP Production for the Common Metabolic Pathway. The Importance of ATP. Non-ETC Oxygen-Consuming Reactions. CHEMICAL CONNECTIONS: Cyanide Poisoning; Brown Fat, Newborn Babies, and Hibernating Animals; Flavonoids: An Important Class of Dietary Antioxidants. 24. Carbohydrate Metabolism. Digestion and Absorption of Carbohydrates. Glycolysis. Fates of Pyruvate. ATP Production for the Complete Oxidation of Glucose. Glycogen Synthesis and Degradation. Gluconeogenesis. Terminology for Glucose Metabolic Pathways. The Pentose Phosphate Pathway. CHEMISTRY AT A GLANCE: Glucose Metabolism. Hormonal Control of Carbohydrate Metabolism. CHEMICAL CONNECTIONS: Lactate Accumulation; Diabetes Mellitus. 25. Lipid Metabolism. Digestion and Absorption of Lipids. Triacylglycerol Storage and Mobilization. Glycerol Metabolism. Oxidation of Fatty Acids. ATP Production from Fatty Acid Oxidation. Ketone Bodies. Biosynthesis of Fatty Acids: Lipogenesis. Relationships Between Lipogenesis and Citric Acid Cycle Intermediates. Biosynthesis of Cholesterol. CHEMISTRY AT A GLANCE: Interrelationships Between Carbohydrate and Lipid Metabolism. Relationships Between Lipid and Carbohydrate Metabolism. CHEMICAL CONNECTIONS: High-Intensity Versus Low-Intensity Workouts; Statins: Drugs That Lower Plasma Levels of Cholesterol. 26. Protein Metabolism. Protein Digestion and Absorption. Amino Acid Utilization. Transamination and Oxidative Deamination. The Urea Cycle. Amino Acid Carbon Skeletons. Amino Acid Biosynthesis. Hemoglobin Catabolism. CHEMISTRY AT A GLANCE: Interrelationships Among Carbohydrate, Lipid, and Protein Metabolism. Interrelationships Among Metabolic Pathways. CHEMICAL CONNECTIONS: The Chemical Composition of Urine Arginine, Citrulline, and the Chemical Messenger Nitric Oxide. Answers to Selected Exercises A-1. 2013, 1056pp, Paperback, 9781133106869 INTRODUCTION TO GENERAL, ORGANIC AND BIOCHEMISTRY, INTERNATIONAL EDITION, 10E Frederick A. Bettelheim, Adelphi University; William H. Brown, Beloit College; Mary K. Campbell, Mount Holyoke College; Shawn O. Farrell, Colorado State University This bestselling text continues to lead the way with a strong focus on current issues, pedagogically rich framework, wide variety of medical and biological applications, visually dynamic art program, and exceptionally strong and varied end-of-chapter problems. Revised and updated throughout, the tenth edition now includes new biochemistry content, new Chemical Connections essays, new and revised problems, and more. Every problem from the tenth edition is now available in the OWL online learning system. NEW TO THIS EDITION Ten percent of the book s problems are new or revised. In addition, all problems in the tenth edition are now available in the OWL online learning system. New Chemical Connections boxes such as, DDT, A Boon and a Curse, From Moldy Clover to a Blood Thinner, and Is There a Connection Between Carbohydrates and Obesity? have been added to the text s more than 150 Chemical Connections essays. 9

End-of-chapter problems associated with Chemical Connections are now keyed to provide students with immediate reinforcement. New up-to-date biochemistry coverage includes material on Membrane Cholesterol Function (Chapter 21), Transition Metals and Their Effect on the Structure of Proteins (Chapter 22), Enzyme Inhibitors in Medicine (Chapter 23), Obesity and Type-II Diabetes (Chapter 24), Synthetic Genome (Chapter 26), Nutrient Deficiencies Linked to Depression (Chapter 30), and Immunization (Chapter 31). Coverage of balancing chemical equations now appears earlier in Chapter 4, Chemical Reactions, and the more difficult calculations involving mass relationships have been moved to the end of the chapter. Allotropes of carbon are now included in an expanded Section 5.9, What Are the Characteristics of the Various Types of Solids? Chapter 8, Acids and Bases, now covers the Activity Series. A new How To box in Chapter 11 emphasizes the skills students need to master How to Draw Alternative Chair Conformations of Cyclohexane. Organic mechanisms are now simplified into easy-toremember steps: add a proton, take a proton away, break a bond, and make a bond in Chapter 12, Alkenes and Alkynes. An enhanced version of the OWL online learning system now includes Interactive Examples from the text and more parameterized end-of-chapter questions that encourage students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. In addition, OWL now includes a multimedia ebook, the interactive customizable Cengage YouBook, as well as an optional Solutions Manual ebook. 1. Matter, Energy, and Measurement. 2. Atoms. 3. Chemical Bonds. 4. Chemical Reactions. 5. Gases, Liquids, and Solids. 6. Solutions and Colloids. 7. Reaction Rates and Chemical Equilibrium. 8. Acids and Bases. 9. Nuclear Chemistry. 10. Organic Chemistry. 11. Alkanes. 12. Alkenes and Alkynes. 13. Benzene and Its Derivatives. 14. Alcohols, Ethers, and Thiols. 15. Chirality: The Handedness of Molecules. 16. Amines. 17. Aldehydes and Ketones. 18. Carboxylic Acids. 19. Carboxylic Anhydrides, Esters, and Amides. 20. Carbohydrates. 21. Lipids. 22. Proteins. 23. Enzymes. 24 Chemical Communications: Neurotransmitters and Hormones. 25. Nucleotides, Nucleic Acids, and Heredity. 26. Gene Expression and Protein Synthesis. 27. Bioenergetics: How the Body Converts Food to Energy. 28. Specific Catabolic Pathways: Carbohydrate, Lipid, and Protein Metabolism. 29. Biosynthetic Pathways. 30. Nutrition. 31. Immunochemistry. 32. Body Fluids. (Chapter 32 can be found on this book s companion website, which is accessible from http://www.cengage. com/chemistry/bettelheim) Appendix 1. Exponential Notation. Appendix 2. Significant Figures. Answers to In-Text and Odd-Numbered End-of-Chapter Problems. Glossary. Credits. Index. 2013, 1008pp, Paperback, 9781133109112 INTRODUCTION TO ORGANIC AND BIOCHEMISTRY, 8E Frederick A. Bettelheim, Adelphi University; William H. Brown, Beloit College; Mary K. Campbell, Mount Holyoke College; Shawn O. Farrell, Colorado State University This innovative partial version of INTRODUCTION TO GENERAL, ORGANIC, AND BIOCHEMISTRY gives students a solid foundation of the chemistry of the human body, consistently demonstrating that a strong background in molecular structure and properties leads to better understanding of biochemical interactions. NEW TO THIS EDITION Ten percent of the book s problems are either new or revised. In addition, all problems in the 8th Edition are now available in the OWL online learning system. New Chemical Connections boxes, such as, DDT, A Boon and a Curse, From Moldy Clover to a Blood 10

Thinner, and Is There a Connection Between Carbohydrates and Obesity? have been added. End-of-chapter problems associated with Chemical Connections are now keyed to provide students with immediate reinforcement. New up-to-date biochemistry coverage includes material on Membrane Cholesterol Function, Transition Metals and Their Effect on the Structure of Proteins, Enzyme Inhibitors in Medicine, Obesity and Type-II Diabetes, Synthetic Genome, Nutrient Deficiencies Linked to Depression, and Immunization. New up-to-date biochemistry coverage includes material on Membrane Cholesterol Function, Transition Metals and Their Effect on the Structure of Proteins, Enzyme Inhibitors in Medicine, Obesity and Type-II Diabetes, Synthetic Genome, Nutrient Deficiencies Linked to Depression, and Immunization. Organic mechanisms have been simplified into easyto-remember steps: add a proton, take a proton away, break a bond and make a bond in Chapter 3, Alkenes and Alkynes. An enhanced version of the OWL online learning system now includes Interactive Examples from the text and more parameterized end-of-chapter questions that encourage students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. In addition, OWL now includes a multimedia ebook, the interactive customizable Cengage YouBook, as well as an optional Solutions Manual ebook. 1. Organic Chemistry. 2. Alkanes. 3. Alkenes and Alkynes. 4. Benzene and Its Derivatives. 5. Alcohols, Ethers, and Thiols. 6. Chirality: The Handedness of Molecules. 7. Acids and Bases. 8. Amines. 9. Aldehydes and Ketones 10. Carboxylic Acids. 11. Carboxylic Anhydrides, Esters, and Amides. 12. Carbohydrates. 13. Lipids. 14. Proteins. 15. Enzymes. 16. Chemical Communications: Neurotransmitters and Hormones. 17. Nucleotides, Nucleic Acids, and Heredity. 18. Gene Expression and Protein Synthesis. 19. Bioenergetics: How the Body Converts Food to Energy. 20. Specific Catabolic Pathways: Carbohydrate, Lipid, and Protein Metabolism. 21. Biosynthetic Pathways. 22. Nutrition. 23. Immunochemistry. 24. Body Fluids. (This chapter can be found on this book s companion website, which is accessible from www.cengage.com/chemistry/ bettelheim) Appendix 1. Exponential Notation. Appendix 2. Significant Figures. Answers to In-Text and Odd- Numbered End-of-Chapter Problems. Glossary. Credits. Index. 2013, 704pp, Hardback, 9781133109761 INTRODUCTORY CHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 7E Spencer L. Seager, Weber State University; Michael R. Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh s INTRODUCTORY CHEMISTRY FOR TODAY, 7e, International Edition continues to meet students needs through diverse applications, examples, boxes, and outstanding technology tools. Prompts throughout the new edition lead students to OWL (web-based learning system) two unique online programs that extend the lessons of the text and help students study smarter. In addition to the many resources found in OWL, the book and website contain questions modeled after the Nursing School and Allied Health Entrance Exams. INTRODUCTORY CHEMISTRY FOR TODAY, 7e, International Edition dispels students inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skills the skills necessary for student success. By demonstrating the importance of chemistry concepts to students future careers and by providing important career information online, the authors not only help students set goals but also help them focus on achieving them. 11

NEW TO THIS EDITION ALLIED HEALTH CONNECTION. An expanded Allied-Health Exam Connection section follows the exercises of each chapter and includes examples of chemistry questions found on typical entrance examinations used to screen applicants to Allied- Health professional programs. UPDATED ART AND PHOTOGRAPHY PROGRAM. In addition to adding many new photos to illustrate key concepts, explanations of figures are now incorporated into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. OWL ONLINE LEARNING INTEGRATION. The new edition now contains algorithmically generated versions of most of the end-of-chapters question from the text. NEW AND UPDATED BOXED. New At the Counter boxes focus on drugs and products found on drugstore shelves and at the pharmacy; Chemistry Around Us boxes present everyday applications of chemistry; and updated Chemistry and Your Health boxes relate to students health and the health of the patients that they may care for in their future roles as a part of the allied health work force. NEW END-OF-CHAPTER EXERCISES. A significant number of the end-of-chapter questions are new. A WEALTH OF END-OF-CHAPTER EXERCISES. The book s wide range of end-of-chapter exercises include Additional Exercises that are not tied to a specific section and often consist of problems that integrate several concepts and Chemistry for Thought exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. INTEGRATED LEARNING OBJECTIVES. The book s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter s key skills and concepts. LEARNING CHECKS. These short, self-check exercises follow the book s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. CONCEPT SUMMARY SECTIONS. These end-ofchapter sections summarize each chapter s key concepts and include one or two appropriate endof-chapter exercises per concept. By solving these exercises, students will have an approximate but quick assessment of how well they understand the Learning Objective related to that concept. HOW REACTIONS OCCUR SECTIONS. These sections present the mechanisms of representative organic reactions to help dispel the mystery of how these reactions take place. 1. Matter, Measurements, and Calculations. 2. Atoms and Molecules. 3. Electronic Structure and the Periodic Law. 4. Forces Between Particles. 5. Chemical Reactions. 6. The States of Matter. 7. Solutions and Colloids. 8. Reaction Rates and Equilibrium. 9. Acids, Bases, and Salts. 10. Radioactivity and Nuclear Processes. 11. Organic Compounds: Alkanes. 12. Unsaturated Hydrocarbons. Appendix A: The International System of Measurements. Appendix B: Answers to Even- Numbered End-of-Chapter Exercises. Appendix C: Solutions to Learning Checks. Glossary. Index. 2011, 496pp, Paperback, 9780538734868 INTRODUCTORY CHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 8E Spencer L. Seager, Weber State University; Michael R. Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh s INTRODUCTORY CHEMISTRY FOR TODAY, 8E, International Edition meets students needs through diverse applications, examples, boxes, interactive technology tools, and -- new to this edition -- real life case studies. The Eighth Edition dispels students 12

inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skills--the skills necessary for student success. By demonstrating the importance of chemistry concepts to students future careers, the authors not only help students set goals, but also help them focus on achieving them. NEW TO THIS EDITION CASE STUDIES/CASE STUDY FOLLOW UPS: New Case Studies open each chapter with real life scenarios that students may encounter at home and at work. Each case study incorporates critical chemistry concepts from the chapter in an exciting real life scenario in which the reader feels as if they are a part of the experience. The case studies require the student to make a decision about what they would do if they were in that situation. A follow up to each Case Study appears at the end of each chapter. ASK THE EXPERT: Featured on both the book cover and woven throughout the text the Ask the Expert boxes begin with important questions about nutrition and fitness as related to chemistry--questions that students need to ask and need to know the answers to. The Ask the Expert questions and answers are written by CNN Doctor Melina D. Jampolis--one of the leading Nutrition and Fitness experts in the country. NEW END-OF-CHAPTER EXERCISES: A significant number of the end-of-chapter questions are new. ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Eighth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self-Assessments, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable ipad-compatible multimedia ebook, and an optional Solutions Manual ebook. A UNIQUE AND INSTRUCTIVE ART PROGRAM: Talking Labels in the art itself walk students through each figure, pointing out what they need to see. Explanations of figures are incorporated into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. STUDENT-FOCUSED BOXED : New Ask the Expert boxes written by CNN Nutrition and Fitness Expert Melina D. Jampolis, M.D. discuss important questions and answers about nutrition and fitness as related to chemistry; At the Counter boxes focus on drugs and products found on drugstore shelves and at the pharmacy; Chemistry Around Us boxes present everyday applications of chemistry; and updated Chemistry and Your Health boxes relate to students health and the health of the patients that they may care for in their future roles as a part of the allied health work force. A WEALTH OF END-OF-CHAPTER EXERCISES: The book s wide range of end-of-chapter exercises include Additional Exercises that are not tied to a specific section and often consist of problems that integrate several concepts and Chemistry for Thought exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. ALLIED HEALTH CONNECTION: An Allied-Health Exam Connection section follows each chapter s endof-chapter exercises and includes chemistry questions found on entrance examinations used to screen applicants applying to Allied-Health professional programs. INTEGRATED LEARNING OBJECTIVES: The book s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter s key skills and concepts. LEARNING CHECKS: These short, self-check exercises follow the book s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. 1. Matter, Measurements, and Calculations. 2. Atoms and Molecules. 3. Electronic Structure and the Periodic Law. 4. Forces Between Particles. 5. Chemical Reactions. 6. The States of Matter. 7. Solutions and Colloids. 8. Reaction Rates and Equilibrium. 9. Acids, Bases, and Salts. 10. Radioactivity and Nuclear Processes. 11. Organic Compounds: Alkanes. 12. Unsaturated 13

Hydrocarbons. 13. Alcohols, Phenols, and Ethers. 14. Aldehydes and Ketones. 15. Carboxylic Acids and Esters. 16. Amines and Amides. 17. Carbohydrates. 18. Lipids. 19. Proteins. 20. Enzymes. 21. Nucleic Acids and Protein Synthesis. 22. Nutrition and Energy for Life. 23. Carbohydrate Metabolism. 24. Lipid and Amino Acid Metabolism. 25. Body Fluids. Appendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered End-of-Chapter Exercises. Appendix C: Solutions to Learning Checks. Glossary. Index. 2014, 528pp, Paperback, 9781133605119 LABORATORY EXPERIMENTS FOR INTRODUCTION TO GENERAL, ORGANIC AND BIOCHEMISTRY, INTERNATIONAL EDITION, 8E Frederick A. Bettelheim, Adelphi University; Joseph M. Landesberg, Adelphi University The 48 experiments in this well-conceived manual illustrate important concepts and principles in general, organic, and biochemistry. As in previous editions, three basic goals guided the development of all the experiments: (1) the experiments illustrate the concepts learned in the classroom; (2) the experiments are clearly and concisely written so that students will easily understand the task at hand, will work with minimal supervision because the manual provides enough information on experimental procedures, and will be able to perform the experiments in a 2-1/2 hour laboratory period; and (3) the experiments are not only simple demonstrations, but also contain a sense of discovery. This edition includes many revised experiments and two new experiments. NEW TO THIS EDITION Many of the experiments have been updated. Two new experiments Beer s Law and Standard Curves, and Tyrosinase Enzyme Kinetics have been added. Many of the pre- and post-lab questions have been revised. The 48 experiments in this manual illustrate important concepts and principles in general, organic, and biochemistry. The experiments illustrate the concepts learned in the classroom, and are clearly and concisely written. The experiments are not only simple demonstrations, but also contain a sense of discovery. Experiment 1: Laboratory Techniques: Using the Laboratory Gas Burner; Making Laboratory Measurements Experiment 2: Density Determination Experiment 3: Separation of the Components of a Mixture Experiment 4: Resolution of a Mixture by Distillation Experimnet 5: The Empirical Formula of a Compound: The Law of Constant Composition Experiment 6: Determination of the Formula of a Metal Oxide Experiment 7: Classes of Chemical Reactions Experiment 8: Chemical Properties of Consumer Products Experiment 9: Calorimetry: The Determination of the Specific Heat of a Metal Experimment 10: Boyle s Law: The Pressure Volume Relationship of a Gas Experiment 11: Charles s Law: The Volume Temperature Relationship of a Gas Experiment 12: Properties of Gases: Determination of the Molar Mass of a Volatile Liquid Experiment 13: Physical Properties of Chemicals: Melting Point, Sublimation, and Boiling Point Experiment 14: Solubility and Solutions Experiment 15: Water of Hydration Experiment 16: Factors Affecting Reaction Rates Experiment 17: The Law of Chemical Equilibrium and Le Chatelier s Principle Experiment 18: ph and Buffer Solutions Experiment 19: Analysis of Vinegar by Titration Experiment 20: Analysis of Antacid Tablets Experiment 21: Structure in Organic Compounds: Use of Molecular Models. I Experiment 22: Stereochemistry: Use of Molecular Models. II Experiment 23: Column and Paper Chromatography: Separation of Plant Pigments Experiment 24: Classification and Identification of Hydrocarbons Experiment 25: Classification and Identification of Alcohols and Phenols Experiment 14

26: Classification and Identification of Aldehydes and Ketones Experiment 27: Properties of Carboxylic Acids and Esters Experiment 28: Properties of Amines and Amides Experiment 29: Polymerization Reactions Experiment 30: Preparation of Acetylsalicylic Acid (Aspirin) Experiment 31: Isolation of Caffeine from Tea Leaves Experiment 32: Carbohydrates Experiment 33: Fermentation of a Carbohydrate:Ethanol from Sucrose Experiment 34: Preparation and Properties of a Soap Experiment 35: Preparation of a Hand Cream Experiment 36: Extraction and Identification of Fatty Acids from Corn Oil Experiment 37: Analysis of Lipids Experimnet 38: Separation of Amino Acids by Paper Chromatography Experiment 39: Acid Base Properties of Amino Acids Experiment 40: Isolation and Identification of Casein Experiment 41: Properties of Enzymes Experiment 42: Neurotransmission: An Example of Enzyme Specificity Experiment 43: Isolation and Identification of DNA from Onion Experiment 44: Viscosity and Secondary Structure of DNA Experiment 45: Beer s Law and Standard Curves Experiment 46: Tyrosinase Enzyme Kinetics Experiment 47: Quantitative Analysis of Vitamin C Contained in Foods Experiment 48: Analysis of Vitamin A in Margarine 2013, 656pp, Paperback, 9781133113102 ORGANIC AND BIOCHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 7E Spencer L. Seager, Weber State University; Michael R. Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh s ORGANIC AND BIOCHEMISTRY FOR TODAY, 7e, International Edition continues to meet students needs through diverse applications, examples, boxes, and outstanding technology tools and now offers an updated and improved art program. Prompts throughout the new edition lead students to OWL (webbased learning system) two unique online programs that extend the lessons of the text and help students study smarter. In addition to the many resources found in CengageNOW and OWL, the book and website contain questions modeled after the Nursing School and Allied Health Entrance Exams. ORGANIC AND BIOCHEMISTRY FOR TODAY, 7e, International Edition dispels students inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skills the skills necessary for student success. By demonstrating the importance of chemistry concepts to students future careers and by providing important career information online, the authors not only help students set goals but also help them focus on achieving them. NEW TO THIS EDITION ALLIED HEALTH CONNECTION. An expanded Allied-Health Exam Connection section follows the exercises of each chapter and includes examples of chemistry questions found on typical entrance examinations used to screen applicants to Allied- Health professional programs. UPDATED ART AND PHOTOGRAPHY PROGRAM. In addition to adding many new photos to illustrate key concepts, explanations of figures are now incorporated into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. OWL ONLINE LEARNING INTEGRATION. The new edition now contains algorithmically generated versions of most of the end-of-chapters question from the text. NEW AND UPDATED BOXED. New At the Counter boxes focus on drugs and products found on drugstore shelves and at the pharmacy; Chemistry Around Us boxes present everyday applications of chemistry; and updated Chemistry and Your Health boxes relate to students health and the health of the patients that they may care for in their future roles as a part of the allied health work force. 15

NEW END-OF-CHAPTER EXERCISES. A significant number of the end-of-chapter questions are new. A WEALTH OF END-OF-CHAPTER EXERCISES. The book s wide range of end-of-chapter exercises include Additional Exercises that are not tied to a specific section and often consist of problems that integrate several concepts and Chemistry for Thought exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. INTEGRATED LEARNING OBJECTIVES. The book s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter s key skills and concepts. LEARNING CHECKS. These short, self-check exercises follow the book s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. CONCEPT SUMMARY SECTIONS. These end-ofchapter sections summarize each chapter s key concepts and include one or two appropriate endof-chapter exercises per concept. By solving these exercises, students will have an approximate but quick assessment of how well they understand the Learning Objective related to that concept. HOW REACTIONS OCCUR SECTIONS. These sections present the mechanisms of representative organic reactions to help dispel the mystery of how these reactions take place. 1. Organic Compounds: Alkanes. 2. Unsaturated Hydrocarbons. 3. Alcohols, Phenols, and Ethers. 4. Aldehydes and Ketones. 5. Carboxylic Acids and Esters. 6. Amines and Amides. 7. Carbohydrates. 8. Lipids. 9. Proteins. 10. Enzymes. 11. Nucleic Acids and Protein Synthesis. 12. Nutrition and Energy for Life. 13. Carbohydrate Metabolism. 14. Lipid and Amino Acid Metabolism. 15. Body Fluids. Appendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered End-of-Chapter Exercises. Appendix C: Solutions to Learning Checks. Glossary. Index. 2011, 512pp, Paperback, 9780538734851 ORGANIC AND BIOCHEMISTRY FOR TODAY, INTERNATIONAL EDITION, 8E Spencer L. Seager, Weber State University; Michael R. Slabaugh, Weber State University Distinguished by its superior allied health focus and integration of technology, Seager and Slabaugh s ORGANIC AND BIOCHEMISTRY FOR TODAY, 8E, International Edition meets students needs through diverse applications, examples, boxes, interactive technology tools, and -- new to this edition -- real life case studies. The Eighth Edition dispels students inherent fear of chemistry and instills an appreciation for the role chemistry plays in our daily lives through a rich pedagogical structure and an accessible writing style with lucid explanations. In addition, the book provides greater support in both problem-solving and critical-thinking skills--the skills necessary for student success. By demonstrating the importance of chemistry concepts to students future careers, the authors not only help students set goals, but also help them focus on achieving them. NEW TO THIS EDITION CASE STUDIES AND CASE STUDY FOLLOW UPS: New Case Studies open each chapter with real life scenarios that students may encounter at home and at work. Each case study incorporates critical chemistry concepts from the chapter in an exciting real life scenario in which readers feel as if they are a part of the experience. The case studies require students to make a decision about what they would do if they were in that situation. A follow up to each Case Study appears at the end of each chapter. ASK THE EXPERT BOXES: Featured on both the book cover and woven throughout the text the Ask the Expert boxes begin with important questions about nutrition and fitness as related to chemistry- 16

-questions that students need to ask and need to know the answers to. The Ask the Expert questions and answers are written by CNN Doctor Melina D. Jampolis--one of the leading Nutrition and Fitness experts in the country. NEW END-OF-CHAPTER EXERCISES: A significant number of the end-of-chapter questions are new. ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Eighth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self-Assessments, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable ipad-compatible multimedia ebook, and an optional Solutions Manual ebook. A UNIQUE AND INSTRUCTIVE ART PROGRAM: Talking Labels in the art itself walk students through each figure, pointing out what they need to see. Explanations of figures are incorporated into the art, rather than appearing in the caption, to help students follow processes and understand exactly what is happening within each figure without having to go back and forth between figure and caption. STUDENT-FOCUSED BOXED : New Ask the Expert boxes written by CNN Nutrition and Fitness Expert Melina D. Jampolis, M.D. discuss important questions and answers about nutrition and fitness as related to chemistry; At the Counter boxes focus on drugs and products found on drugstore shelves and at the pharmacy; Chemistry Around Us boxes present everyday applications of chemistry; and updated Chemistry and Your Health boxes relate to students health and the health of the patients that they may care for in their future roles as a part of the allied health work force. A WEALTH OF END-OF-CHAPTER EXERCISES: The book s wide range of end-of-chapter exercises include Additional Exercises that are not tied to a specific section and often consist of problems that integrate several concepts and Chemistry for Thought exercises that focus on conceptual and cumulative questions and ask students to apply what they have learned to a particular cumulative question. ALLIED HEALTH CONNECTION: An Allied-Health Exam Connection section follows each chapter s endof-chapter exercises and includes chemistry questions found on entrance examinations used to screen applicants applying to Allied-Health professional programs. INTEGRATED LEARNING OBJECTIVES: The book s Learning Objectives are integrated throughout each chapter and within the summary to help students focus on the chapter s key skills and concepts. LEARNING CHECKS: These short, self-check exercises follow the book s worked-out examples and discussions of key or difficult concepts to help students assess their understanding. 1. Organic Compounds: Alkanes. 2. Unsaturated Hydrocarbons. 3. Alcohols, Phenols, and Ethers. 4. Aldehydes and Ketones. 5. Carboxylic Acids and Esters. 6. Amines and Amides. 7. Carbohydrates. 8. Lipids. 9. Proteins. 10. Enzymes. 11. Nucleic Acids and Protein Synthesis. 12. Nutrition and Energy for Life. 13. Carbohydrate Metabolism. 14. Lipid and Amino Acid Metabolism. 15. Body Fluids. Appendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered End-of-Chapter Exercises. Appendix C: Solutions to Learning Checks. Glossary. Index. 2014, 544pp, Paperback, 9781133607496 ORGANIC AND BIOLOGICAL CHEMISTRY, 6E H. Stephen Stoker, Weber State University This text is comprised of Chapters 12-26 of Stoker s, GENERAL, ORGANIC, AND BIOLOGICAL CHEMISTRY, 6e. Like the longer book, ORGANIC AND BIOLOGICAL 17

CHEMISTRY, 6e emphasizes the applications of chemistry, minimizes complicated mathematics, and is written throughout to help students succeed in the course and master the biochemistry content that is so important to their future careers. The Six Edition s clear explanations, visual support, and effective pedagogy combine to make the text ideal for allied health majors. NEW TO THIS EDITION Several new Chemistry At-A-Glance boxes covering critical chemistry concepts have been added to this edition. New Chemical Connection Boxes covering a variety of topics that relate chemistry to our everyday lives! Heavily revised art and photography program. Talking labels have been added to many of the illustrations these labels help students understand the concepts being discussed in the figure. New questions and problems have been added to the end of chapter question/problem sets including a new type of problem that is related to the Chemical Connection boxes the new questions are identified with an icon. Up to date coverage throughout the text, but especially the biochemistry chapters. Biochemistry is an ever changing field and the new edition has been updated with the latest information in that field. OWL and Youbook: OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. Also includes Student Self Assessments, the interactive customizable Cengage YouBook, and an optional Solutions Manual ebook. Chemistry at-a-glance features provide brief visual summaries of core chapter concepts to help students visualize difficult material. Chemical Connection Boxes show chemistry as it relates to everyday life, highlighting its relevance to students future careers in the health and environmental fields. A wide range of examples throughout the book help students improve their problem-solving skills. Look-back, look-forward marginal notes show students where General, Organic, and Biochemistry topics connect. Part I: ORGANIC CHEMISTRY. 1. Saturated Hydrocarbons Organic and Inorganic Compounds. Bonding Characteristics of the Carbon Atom. Hydrocarbons and Hydrocarbon Derivatives. Alkanes: Acyclic Saturated Hydrocarbons. Structural Formulas. Alkane Isomerism. Conformations of Alkanes. IUPAC Nomenclature for Alkanes. Line-Angle Formulas for Alkanes. Classification of Carbon Atoms. Branched-Chain Alkyl Groups. Cycloalkanes. IUPAC Nomenclature for Cycloalkanes. Isomerism in Cycloalkanes. Sources of Alkanes and Cycloalkanes. Physical Properties of Alkanes and Cycloalkanes. Chemical Properties of Alkanes and Cycloalkanes. Chemistry at a Glance: Properties of Alkanes and Cycloalkanes. Nomenclature and Properties of Halogenated Alkanes. Chemical Connections: The Occurrence of Methane; The Physiological Effects of Alkanes; Chlorofluorocarbons and the Ozone Layer. 2. Unsaturated Hydrocarbons. Unsaturated Hydrocarbons. Characteristics of Alkenes and Cycloalkenes. Names for Alkenes and Cycloalkenes. Line-Angle Formulas for Alkenes. Isomerism in Alkenes. Naturally Occurring Alkenes. Physical Properties of Alkenes. Chemical Reactions of Alkenes. Polymerization of Alkenes: Addition Polymers. Alkynes. Chemistry at a Glance: Chemical Reactions of Alkenes. Chemistry at a Glance: IUPAC Nomenclature for Alkanes, Alkenes, and Alkynes. Aromatic Hydrocarbons. Names for Aromatic Hydrocarbons. Aromatic Hydrocarbons: Physical Properties and Sources. Chemical Reactions of Aromatic Hydrocarbons. Fused-Ring Aromatic Compounds. Chemical Connections: Ethene: A Plant Hormone and High-Volume Industrial Chemical; Cis-Trans Isomerism and Vision; Carotenoids: A Source of Color; Fused-Ring Aromatic Hydrocarbons and Cancer. 3. Alcohols, Phenols, and Ethers Bonding Characteristics of Oxygen Atoms in Organic Compounds. Structural Characteristics of Alcohols. Nomenclature for Alcohols. Isomerism for Alcohols. Important Commonly Encountered Alcohols. Physical Properties of Alcohols. Preparation of Alcohols. Classification of Alcohols. Chemical Reactions of Alcohols. Chemistry at a Glance: Summary of Chemical Reactions Involving Alcohols. Polymeric Alcohols. Structural Characteristics of Phenols. Nomenclature for Phenols. Physical and Chemical Properties of Phenols. Occurrence of and Uses for Phenols. Structural 18

Characteristics of Ethers. Nomenclature for Ethers. Isomerism for Ethers. Physical and Chemical Properties of Ethers. Cyclic Ethers. Sulfur Analogs and Alcohols. Sulfur Analogs of Ethers. Chemical Connections: Menthol: A Useful Naturally Occurring Terpene Alcohol; Ethers as General Anesthetics; Marijuana: The Most Commonly Used Illicit Drug; Garlic and Onions: Odiferous Medicinal Plants. 4. Aldehydes and Ketones. The Carbonyl Group. Structure of Aldehydes and Ketones. Nomenclature for Aldehydes. Nomenclature for Ketones. Isomerism for Aldehydes and Ketones. Selected Common Aldehydes and Ketones. Physical Properties of Aldehydes and Ketones. Preparation of Aldehydes and Ketones. Oxidation and Reduction of Aldehydes and Ketones. Reaction of Aldehydes and Ketones with Alcohols. Chemistry at a Glance: Summary of Chemical Reactions Involving Aldehydes and Ketones. Formaldehyde-Based Polymers. Sulfur-Containing Carbonyl Groups. Chemical Connections: Lachrymatory Aldehydes and Ketones; Melanin: A Hair and Skin Pigment; Diabetes, Aldehyde Oxidation, and Glucose Testing. 5. Carboxylic Acids, Esters, and Other Acid Derivatives. Structure of Carboxylic Acids and Their Derivatives. IUPAC Nomenclature for Carboxylic Acids. Common Names for Carboxylic Acids. Polyfunctional Carboxylic Acids. Metabolic Acids. Physical Properties of Carboxylic Acids. Preparation of Carboxylic Acids. Acidity of Carboxylic Acids. Carboxylic Acid Salts. Structure of Esters. Preparation of Esters. Chemistry at a Glance: Summary of the H Versus R Relationship for Pairs of Hydrocarbon Derivatives. Nomenclature for Esters. Selected Common Esters. Isomerism for Carboxylic Acids and Esters. Physical Properties of Esters. Chemical Reactions of Esters. Sulfur Analogs of Esters. Polyesters. Chemistry at a Glance: Summary of Chemical Reactions Involving Carboxylic Acids and Esters. Acid Chlorides and Acid Anhydrides. Esters and Anhydrides of Inorganic Acids. Chemical Connections: Nonprescription Pain Relievers Derived from Propanoic Acid; Carboxylic Acids and Skin Care; Aspirin; Nitroglycerin: An Inorganic Triester. 6. Amines and Amides. Bonding Characteristics of Nitrogen Atoms in Organic Compounds. Structure and Classification of Amines. Nomenclature for Amines. Isomerism for Amines. Physical Properties of Amines. Basicity of Amines. Amine Salts. Heterocyclic Amines. Selected Biochemically Important Amines. Alkaloids. Structure and Classification of Amides. Nomenclature for Amides. Selected Amides and Their Uses. Properties of Amides. Preparation of Amides. Hydrolysis of Amides. Polyamides and Polyurethanes. Chemistry at a Glance: Summary of Chemical Reactions Involving Amines and Amides. Chemical Connections: Caffeine: The Most Widely Used Central Nervous System Stimulant; Amphetamines: Central Nervous System Stimulants; Alkaloids Present in Chocolate; Acetaminophen: A Substituted Amide. Part II: BIOLOGICAL CHEMISTRY. 7. Carbohydrates. Biochemistry An Overview. Occurrence and Functions of Carbohydrates. Classification of Carbohydrates. Chirality: Handedness in Molecules. Stereoisomerism: Enantiomers and Diastereomers. Designating Handedness Using Fischer Projections. Chemistry at a Glance: Constitutional Isomers and Stereoisomers. Properties of Enantiomers. Classification of Monosaccharides. Biochemically Important Monosaccharides. Cyclic Forms of Monosaccharides. Haworth Projection Formulas. Reactions of Monosaccharides. Disaccharides. Chemistry at a Glance: Sugar Terminology Associated with Monosaccharides and Their Derivatives. General Characteristics of Polysaccharides. Storage Polysaccharides. Structural Polysaccharides. Chemistry at a Glance: Types of Glycosidic Linkages for Common Glucose-Containing Di- and Polysaccharides. Acidic Polysaccharides. Glycolipids and Glycoproteins. Dietary Considerations and Carbohydrates. Chemical Connections: Blood Types and Monosaccharides; Lactose Intolerance and Galactosemia; Artifical Sweeteners; Good and Bad Carbs : The Glycemic Index. 8. Lipids. Structure and Classification of Lipids. Fatty Acids: Lipid Building Blocks. Physical Properties of Fatty Acids. Energy- Storage Lipids: Triacylglycerols. Dietary Considerations and Triacylglycerols. Chemical Reactions of Triacylglycerols. Chemistry at a Glance: Classification Schemes for Fatty Acid Residues Present in Triacylglycerols. Membrane Lipids: Phospholipids. Membrane Lipids: Sphingoglycolipids. Chemistry at a Glance: Terminology for and Structural Relationships Among Various Types of Fatty-Acid-Containing Lipids. Membrane Lipids: Cholesterol. Cell Membranes. Emulsification Lipids: Bile Acids. Messenger Lipids: Steroid Hormones. Messenger Lipids: Eicosanoids. Protective-Coating Lipids: Biological Waxes. Chemistry at a Glance: Types of Lipids and How They Function. 19

Chemical Connections: The Fat Content of Tree Nuts and Peanuts; Artificial Fat Substitutes; The Cleansing Action of Soap; Trans Fatty Acids and Blood Cholesterol Levels; Steroid Drugs in Sports; The Mode of Action for Anti-Inflammatory Drugs. 9. Proteins Characteristics of Proteins. Amino Acids: The Building Blocks for Proteins. Chirality and Amino Acids. Acid-Base Properties of Amino Acids. Cysteine: A Chemically Unique Amino Acid. Peptide Formation. Biochemically Important Small Peptides. General Structural Characteristics of Proteins. Primary Structure of Proteins. Secondary Structure of Proteins. Tertiary Structure of Proteins. Quaternary Structure of Proteins. Fibrous and Globular Proteins. Chemistry at a Glance: Protein Structure. Protein Hydrolysis. Protein Denaturation. Glycoproteins. Lipoproteins. Chemical Connections: The Essential Amino Acids; Substitutes for Human Insulin; Protein Structure and the Color of Meat; Denaturation and Human Hair; Cyclosporine: An Antirejection Drug; Lipoproteins and Heart Attack Risk. 10. Enzymes and Vitamins. General Characteristics of Enzymes. Nomenclature and Classification of Enzymes. Enzyme Structure. Models of Enzyme Action. Enzyme Specificity. Factors That Affect Enzyme Activity. Chemistry at a Glance: Enzyme Activity. Enzyme Inhibition. Regulation of Enzyme Activity: Allosteric Enzymes. Chemistry at a Glance: Enzyme Inhibition. Regulation of Enzyme Activity: Zymogens. Antibiotics That Inhibit Enzyme Activity. Medical Uses of Enzymes. Vitamins. Water- Soluble Vitamins. Fat-Soluble Vitamins. Chemical Connections: H. pylori and Stomach Ulcers; Enzymatic Browning: Discoloration of Fruits and Vegetables; Heart Attacks and Enzyme Analysis. 11. Nucleic Acids. Types of Nucleic Acids. Nucleotides: Building Blocks of Nucleic Acids. Primary Nucleic Acid Structure. The DNA Double Helix. Replication of DNA Molecules. Overview of Protein Synthesis. Ribonucleic Acids. Chemistry at a Glance: DNA Replication. Transcription: RNA Synthesis. The Genetic Code. Anticodons and trna Molecules. Translation: Protein Synthesis. Mutations. Chemistry at a Glance: Protein Synthesis. Nucleic Acids and Viruses. Recombinant DNA and Genetic Engineering. The Polymerase Chain Reaction. DNA Sequencing. Chemical Connections: Use of Synthetic Nucleic Acid Bases in Medicine; Antibiotics That Inhibit Bacterial Protein Synthesis. 12. Biochemical Energy Production. Metabolism. Metabolism and Cell Structure. Important Intermediate Compounds in Metabolic Pathways. High- Energy Phosphate Compounds. An Overview of Biochemical Energy Production. The Citric Acid Cycle. Chemistry at a Glance: Simplified Summary of the Four Stages of Biochemical Energy Production. Chemistry at a Glance: Summary of the Reactions of the Citric Acid Cycle. The Electron Transport Chain. Chemistry at a Glance: Summary of the Flow of Electrons Through the Four Complexes of the Electron Transport Chain. Oxidative Phosphorylation. Chemistry at a Glance: Summary of the Common Metabolic Pathway. ATP Production for the Common Metabolic Pathway. The Importance of ATP. Non-ETC Oxygen-Consuming Reactions. Chemical Connections: Cyanide Poisoning; Brown Fat, Newborn Babies, and Hibernating Animals; Flavonoids: An Important Class of Dietary Antioxidants. 13. Carbohydrate Metabolism. Digestion and Absorption of Carbohydrates. Glycolysis. Fates of Pyruvate. ATP Production for the Complete Oxidation of Glucose. Glycogen Synthesis and Degradation. Gluconeogenesis and the Cori Cycle. Terminology for Glucose Metabolic Pathways. The Pentose Phosphate Pathway. Chemistry at a Glance: Glucose Metabolism. Hormonal Control of Carbohydrate Metabolism. Chemical Connections: Lactate Accumulation; Diabetes Mellitus. 14. Lipid Metabolism. Digestion and Absorption of Lipids. Triacylglycerol Storage and Mobilization. Glycerol Metabolism. Oxidation of Fatty Acids. ATP Production from Fatty Acid Oxidation. Ketone Bodies. Biosynthesis of Fatty Acids: Lipogenesis. Biosynthesis of Cholesterol. Chemistry at a Glance: Interrelationships Between Carbohydrate and Lipid Metabolism. Relationships Between Lipid and Carbohydrate Metabolism. Chemical Connections: High-Intensity Versus Low-Intensity Workouts; Statins: Drugs That Lower Plasma Levels of Cholesterol. 15. Protein Metabolism Protein Digestion and Absorption. Amino Acid Utilization. ransamination and Oxidative Deamination. The Urea Cycle. Amino Acid Carbon Skeletons. Amino Acid Biosynthesis. Hemoglobin Catabolism. Chemistry at a Glance: Interrelationships Among Lipid, Carbohydrate, and Protein Metabolism. Interrelationships Among Metabolic Pathways. Chemical Connections: The Chemical Composition of Urine. Arginine, Citrulline, and the Chemical Messenger Nitric Oxide. 2013, 704pp, Hardback, 9781133103950 20

SAFETY-SCALE LABORATORY EXPERIMENTS FOR CHEMISTRY FOR TODAY, 7E Spencer L. Seager, Weber State University; Michael R. Slabaugh, Weber State University Providing a unique blend of laboratory skills and exercises that illustrate concepts from the authors main text, CHEMISTRY FOR TODAY: GENERAL, ORGANIC, AND BIOCHEMISTRY, 7e, this accurate and well-tested lab manual contains 15 general chemistry and 20 organic/biochemistry safety-scale laboratory experiments. The experiments are designed to use small quantities of chemicals and emphasize safety and proper disposal of materials. Safety-scale is the authors own term for describing the amount of chemicals each lab experiment requires--less than macroscale quantities, which are expensive and hazardous--and more than microscale quantities, which are difficult to work with and require special equipment. NEW TO THIS EDITION ACCURATE AND CLASS-TESTED. The Seventh Edition includes 15 general chemistry and 20 organic/ biochemistry safety-scale laboratory experiments--all thoroughly class-tested--that effectively illustrate the main text s key concepts. A KEY CONCEPT FOCUS: The manual s blend of laboratory skills and exercises illustrate key concepts from the main textbook. BUILT-IN PEDAGOGY: Pre-lab questions prepare students for each lab and end-of-experiment questions assess student understanding. FLEXIBLE AND CONVENIENT. The manual is threehole punched and features perforated pages, which make it easy for student to hand in lab reports and answers to pre- and post-lab questions and exercises upon instructor request. Introduction. Experiment 1: Measurements and Significant Figures. Experiment 2: The Use of Chemical Balances. Experiment 3: The Use of Volumetric Ware and the Determination of Density. Experiment 4: Physical and Chemical Changes. Experiment 5: Separations and Analysis. Experiment 6: Classification of Chemical Reactions. Experiment 7: Analysis Using Decomposition Reactions. Experiment 8: Gas Laws. Experiment 9: Solution Formation and Characteristics. Experiment 10: Colligative Properties of Solutions. Experiment 11: Reactions Rates and Equilibrium. Experiment 12: Acids, Bases, Salts, and Buffers. Experiment 13: Analysis of Vinegar. Experiment 14: Determination of Ka for Weak Acids. Experiment 15: The Acidic Hydrogens of Acids. Experiment 16: The Use of Melting Points in the Identification of Organic Compounds. Experiment 17: Isolation and Purification of an Organic Compound. Experiment 18: Hydrocarbons. Experiment 19: Reactions of Alcohols and Phenols. Experiment 20: Reactions of Aldehydes and Ketones. Experiment 21: Reactions of Carboxylic Acids, Amines, and Amides. Experiment 22: The Synthesis of Aspirin and Other Esters. Experiment 23: Identifying Functional Groups in Unknowns. Experiment 24: Synthetic Polymers. Experiment 25: Dyes, Inks, and Food Colorings. Experiment 26: A Study of Carbohydrates. Experiment 27: Preparations of Soap by Lipid Saponification. Experiment 28: Isolation of Natural Products: Trimyristin and Cholesterol. Experiment 29: Amino Acids and Proteins. Experiment 30: Enzymes: Nature s Catalysts. Experiment 31: Factors That Influence Enzyme Activity. Experiment 32: Vitamin C Content of Foods Part I: Assigned Samples. Experiment 33: Vitamin C Content of Foods Part II: Samples from Home. Experiment 34: Extraction of DNA from Wheat Germ. Experiment 35: Detection of Minerals in Breakfast Cereals. APPENDIX A: Graphs and Graphing. APPENDIX B: Equipment, Chemicals, Reagents, and Supplies. APPENDIX C: Table of Atomic Weights and Numbers. 2011, 544pp, Paperback, 9780538734547 21

SAFETY-SCALE LABORATORY EXPERIMENTS FOR CHEMISTRY FOR TODAY, 8E Spencer L. Seager, Weber State University; Michael R. Slabaugh, Weber State University This proven lab manual offers a unique blend of laboratory skills and exercises that effectively illustrate concepts from the main text, CHEMISTRY FOR TODAY: GENERAL, ORGANIC, AND BIOCHEMISTRY, 8e. The book s 15 general chemistry and 20 organic/ biochemistry safety-scale laboratory experiments use small quantities of chemicals and emphasize safety and proper disposal of materials. Safety-scale is the authors own term for describing the amount of chemicals each lab experiment requires--less than macroscale quantities, which are expensive and hazardous, and more than microscale quantities, which are difficult to work with and require special equipment. NEW TO THIS EDITION Updated and thoroughly reviewed labs. ACCURATE AND CLASS-TESTED. The Eighth Edition includes 15 general chemistry and 20 organic/ biochemistry safety-scale laboratory experiments--all thoroughly class-tested--that effectively illustrate the main text s key concepts. A KEY CONCEPT FOCUS: The manual s blend of laboratory skills and exercises illustrate key concepts from the main textbook. BUILT-IN PEDAGOGY: Pre-lab questions prepare students for each lab and end-of-experiment questions assess student understanding. FLEXIBLE AND CONVENIENT. The manual is threehole punched and features perforated pages, which make it easy for student to hand in lab reports and answers to pre- and post-lab questions and exercises upon instructor request. 1. Matter, Measurements, and Calculations. 2. Atoms and Molecules. 3. Electronic Structure and the Periodic Law. 4. Forces Between Particles. 5. Chemical Reactions. 6. The States of Matter. 7. Solutions and Colloids. 8. Reaction Rates and Equilibrium. 9. Acids, Bases, and Salts. 10. Radioactivity and Nuclear Processes. 11. Organic Compounds: Alkanes. 12. Unsaturated Hydrocarbons. 13. Alcohols, Phenols, and Ethers. 14. Aldehydes and Ketones. 15. Carboxylic Acids and Esters. 16. Amines and Amides. 17. Carbohydrates. 18. Lipids. 19. Proteins. 20. Enzymes. 21. Nucleic Acids and Protein Synthesis. 22. Nutrition and Energy for Life. 23. Carbohydrate Metabolism. 24. Lipid and Amino Acid Metabolism. 25. Body Fluids. Appendix A: The International System of Measurements. Appendix B: Answers to Even-Numbered End-of-Chapter Exercises. Appendix C: Solutions to Learning Checks. Glossary. Index. 2014, 544pp, Paperback, 9781133604259 STUDY GUIDE WITH STUDENT SOLUTIONS MANUAL FOR SEAGER/ SLABAUGH S CHEMISTRY FOR TODAY, 8TH, 8E Spencer L. Seager, Weber State University; Michael R. Slabaugh, Weber State University Study more effectively and improve your performance at exam time with this comprehensive guide. Updated to reflect all changes to the core text, the Eighth Edition tests you on the learning objectives in each chapter and provides answers to all the even-numbered endof-chapter exercises. 2014, 432pp, Paperback, 9781133606994 22

Analytical Chemistry APPLICATIONS OF MICROSOFT EXCEL IN ANALYTICAL CHEMISTRY, 2E F. James Holler, University of Kentucky; Stanley R. Crouch, Michigan State University This supplement can be used in any analytical chemistry course. The exercises teach students how to use Microsoft Excel using applications from statistics, data analysis equilibrium calculations, curve fitting, and more. Operations include everything from basic arithmetic and cell formatting to Solver, Goal Seek, and the Data Analysis Toolpak. The authors show students how to use a spreadsheet to construct log diagrams and to plot the results. Statistical data treatment includes descriptive statistics, linear regression, hypothesis testing, and analysis of variance. Tutorial exercises include nonlinear regression such as fitting the Van Deemter equation, fitting kinetics data, determining error coefficients in spectrophotometry, and calculating titration curves. Additional features include solving complex systems of equilibrium equations and advanced graphical methods: error bars, charts with insets, matrices and determinants, and much more. NEW TO THIS EDITION The description and instructions were completely changed from those of Excel 2003 to Excel 2010 (2007). There is now a better coordination with Skoog, Fundamentals of Analytical Chemistry, 9e in terms of worked examples. The Spreadsheet examples, formerly in the Skoog book were off-loaded to the new Excel book so that the burden for teaching about Excel is now on the Excel book. Precipitation titrations were included in Chapter 9. Descriptions and instructions written so that they can be used with either the Office 2007 or 2010 versions of Excel. Cross references to Skoog Fundamentals of Analytical Chemistry, 9e and Skoog, Analytical Chemistry: An Introduction are included. Exercises teach students how to use Microsoft Excel with applications from statistics, data analysis equilibrium calculations, curve fitting, and more. Operations include everything from basic arithmetic and cell formatting to Solver, Goal Seek, and the Data Analysis Toolpak. The authors show students how to use a spreadsheet to construct log diagrams and to plot the results. Statistical data treatment includes descriptive statistics, linear regression, hypothesis testing, and analysis of variance. Tutorial exercises include nonlinear regression such as fitting the Van Deemter equation, fitting kinetics data, determining error coefficients in spectrophotometry, and calculating titration curves. 1. Excel Basics. 2. Basic Statistical Analysis with Excel. 3. Statistical Tests with Excel. 4. Least-Squares and Calibration Methods. 5. Equilibrium, Activity and Solving Equations. 6. The Systematic Approach to Equilibria: Solving Many Equations. 7. Neutralization Titrations and Graphical Representations. 8. Polyfunctional Acids and Bases. 9. Complexometric and Precipitation Titrations. 10. Potentiometry and Redox Titrations. 11. Dynamic Electrochemistry. 12. Spectrochemical Methods. 13. Kinetic Methods. 14. Chromatography. 15. Electrophoresis and Other Separation Methods. 16. Data Processing with Excel. 2014, 480pp, Paperback, 9781285087955 23

Coming Soon! FUNDAMENTALS OF ANALYTICAL CHEMISTRY, INTERNATIONAL EDITION, 9E Douglas A. Skoog, Stanford University; Donald M. West, San Jose State University; F. James Holler, University of Kentucky; Stanley R. Crouch, Michigan State University Known for its readability and systematic, rigorous approach, this fully updated FUNDAMENTALS OF ANALYTICAL CHEMISTRY, 9E, International Edition offers extensive coverage of the principles and practices of analytic chemistry and consistently shows students its applied nature. The book s award-winning authors begin each chapter with a story and photo of how analytic chemistry is applied in industry, medicine, and all the sciences. To further reinforce student learning, a wealth of dynamic photographs by renowned chemistry photographer Charlie Winters appear as chapteropeners and throughout the text. Incorporating Excel spreadsheets as a problem-solving tool, the Ninth Edition is enhanced by a chapter on Using Spreadsheets in Analytical Chemistry, updated spreadsheet summaries and problems, an Excel Shortcut Keystrokes for the PC insert card, and a supplement by the text authors, EXCEL APPLICATIONS FOR ANALYTICAL CHEMISTRY, which integrates this important aspect of the study of analytical chemistry into the book s already rich pedagogy. New to this edition is OWL, an online homework and assessment tool that includes the Cengage YouBook, a fully customizable and interactive ebook, which enhances conceptual understanding through hands-on integrated multimedia interactivity. NEW TO THIS EDITION OWL (Online Web Learning) is available for the first time with this Ninth Edition. OWL includes parameterized Mastery homework assignments correlated to sections in the text and parameterized end-of-chapter questions. OWL encourages students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes the interactive customizable Cengage YouBook and an optional Solutions Manual ebook. All chapters have been rewritten for Excel 2010 (or 2007). A new Chapter 29 on Mass Spectrometry incorporates atomic mass spectrometry (formerly in Chapter 28) with new material on molecular mass spectrometry. New end-of-chapter problems have been added. All examples are now titled for easy reference. New Feature Boxes appear throughout, such as Feature 14-4 on the Master Equation. Approach. Chapter 17 has a new section on Precipitation Titrations. In Chapter 25, the discussion on thermal IR detectors now puts more emphasis on the DTGS pyroelectric detector. Part VII on Practical Aspects of Chemical Analysis is now online to make it easier for students to access the material on preparing and analyzing real samples. Spreadsheet exercises and problems are integrated into the examples and end-of-chapter material in appropriate chapters to enhance student learning. 1. The Nature of Analytical Chemistry PART I: TOOLS OF ANALYTICAL CHEMISTRY 2. Chemicals, Apparatus, and Unit Operations of Analytical Chemistry 3. Using Spreadsheets in Analytical Chemistry 4. Calculations Used in Analytical Chemistry 5. Errors in Chemical Analyses 6. Random Errors in Chemical Analysis 7. Statistical Data Treatment and Evaluation 8. Sampling, Standardization, and Calibration PART II: CHEMICAL EQUILIBRIA 9. Aqueous Solutions and Chemical Equilibria 10. Effect of Electrolytes on Chemical Equilibria 11. Solving Equilibrium Problems for Complex Systems PART III: CLASSICAL METHODS OF ANALYSIS 12. Gravimetric Methods of Analysis 13. Titrimetric Methods; Precipitation Titrimetry 14. Principles of Neutralization Titrations 15. Titration Curves for Complex Acid/Bases Systems 16. Applications of Neutralization Titrations 17. Complexation Reactions 24

and Titrations PART IV: ELECTROCHEMICAL METHODS 18. Introduction to Electrochemistry 19. Applications of Standard Electrode Potentials 20. Applications of Oxidation/Reduction Titrations 21. Potentiometry 22. Bulk Electrolysis: Electrogravimetry and Coulometry 23. Voltammetry PART V: SPECTROCHEMICAL ANALYSIS 24. Introduction to Spectrochemical Methods 25. Instruments for Optical Spectroscopy 26. Molecular Absorption Spectroscopy 27. Molecular Fluorescence Spectroscopy 28. Atomic Spectroscopy 29. Mass Spectrometry PART VI: KINETICS AND SEPARATIONS 30. Kinetic Methods of Analysis 31. Introduction to Analytical Separations 32. Gas Chromatography 33. High- Performance Liquid Chromatography 34. Miscellaneous Separation Methods PART VII: PRACTICAL ASPECTS OF CHEMICAL ANALYSIS To access the following online-only chapters, enter ISBN 978-0-495-55828-6 at www.cengagebrain.com and visit this book s companion website. 35. Analysis of Real Samples 36. Preparing Samples for Analysis 37. Decomposing and Dissolving the Sample 38. Selected Methods of Analysis 2014, 1072pp, Paperback, 9781285056241 INTRODUCTION TO ANALYTICAL CHEMISTRY Douglas A. Skoog, Stanford University; Donald M. West, San Jose State University; F. James Holler, University of Kentucky; Stanley R. Crouch, Michigan State University <i>introduction to Analytical Chemistry</i> was written with the main aim of providing a strong background in those chemical principles that are important in analytical chemistry. The text covers both fundamental and practical aspects of chemical analysis. The book is organized into five sections; tools of analytical chemistry, principles and applications of chemical equilibrium, electrochemical methods, spectroscopic methods, and separation methods. Molecular models are also used liberally in most chapters to stimulate interest in the beauty of molecular structures and to reinforce structural concepts presented in general chemistry and upper-level courses. The primary audience of this text is non-chemistry majors taking a one-semester course in analytical chemistry. <i>spreadsheet Calculations</i>. Spreadsheet exercises and problems throughout the text show students how to solve problems, conduct graphical analysis, and many other applications using Microsoft Excel. <i>worked Examples</i>. A large number of worked examples serve as aids in understanding the concepts of analytical chemistry. <i>featured Topics</i>. A series of boxed and highlighted features are found throughout the text to arouse students curiosity about real-life applications of analytical chemistry. <i>web Works</i>. In most of the chapters, a brief Web Works feature is included at the end of most chapters. These are urls for websites that provide additional information, alternative discussions, or interesting analytical applications. 1. What is Analytical Chemistry? Section I: The Tools of Analytical Chemistry. 2. Important Chemical Concepts and a Basic Approach to Chemical Equilibrium. 3. Errors, Random Errors, and Statistical Data in Chemical Analyses. Section II: Principles and Applications of Chemical Equilibria. 4. Gravimetric Methods of Analysis. 5. Electrolyte Effects and Equilibrium: Calculations in Complex Systems. 6. Titrations: Taking Advantage of Stoichiometric Reactions. 7. Principles of Neutralization Titrations: Determining Acids, Bases, and the ph of Buffer Solutions. 8.Titrating Polyfunctional Acids and Bases. 9. Applying Neutralization Titrations. 10. Complexation and Precipitation Titrations: Taking Advantage of Complexing and Precipitating Agents. Section III: Electrochemical Methods. 11. Elements of Electrochemistry. 12. Electrode Potentials and Their Applications to Oxidation/Reduction Titrations. 13. Potentiometry: Measuring Concentrations of Ions and Molecules. Section IV: Spectrochemical Analysis. 14. Spectroscopic Methods of Analysis and Instruments for Measuring Absorption. 15. Applying Molecular 25

and Atomic Spectroscopic Methods: Shedding More Light on the Subject. Section V: Separation Methods. 16. An Introduction to Analytical Separations. 17. Chromatographic Methods and Hyphenated Techniques. Web Chapter: 18. Chemicals and Apparaturs: Putting the Tools to Work 19. Hypothesis Testing and Gross Errors. 20. A Brief Look at Some Other Electroanalytical Methods. 21. Supercritical-Fluid Chromatography, Capillary Electrophoreses, and Capillary Electrochromatography. 22. Selected Methods of Analysis. 2011, 660pp, Hardback, 9789814272797 SKOOG AND WEST S FUNDAMENTALS OF ANALYTICAL CHEMISTRY, 9E Cengage Technology Edition Douglas A. Skoog, Stanford University; Donald M. West, San Jose State University; F. James Holler, University of Kentucky; Stanley R. Crouch, Michigan State University This title is a Cengage Technology Edition and offers a blend of print and digital content which has been tailored to meet the demands of today s lecturers and students. Skoog and West s Fundamentals of Analytical Chemistry provides a thorough background in the chemical principles that are particularly important to analytical chemistry. Students using this book will develop an appreciation for the difficult task of judging the accuracy and precision of experimental data and to show how these judgements can be sharpened by applying statistical methods to analytical data. The book introduces a broad range of modern and classic techniques that are useful in analytical chemistry; as well as giving students the skills necessary for both obtaining data in the laboratory and solving quantitative analytical problems. Exclusive photographs taken by renowned chemistry photographer Charlie Winters make it easier for students to understand key principles and processes. Each chapter begins with an application-type photograph and an accompanying relevant and interesting story. Feature boxes throughout the text cover a wide range of topics, including descriptions of Breath Alcohol Analyzers, Lap-on-a-Chip Technology, Modified Electrodes, Enzymatic Determination of Urea, GC/ MS, C/MS, LC/MS/MS, and Capillary Electrophoresis in DNA Sequencing. The art program features Microsoft Excel screenshots, techniques, procedures, and applications with descriptive captions that visually reinforce student understanding. Molecular models, used liberally in most chapters, stimulate interest in the beauty of molecular structures and reinforce structural concepts and descriptive chemistry presented in general chemistry and upper-level courses. A wide spectrum of applications, including developments in biology, medicine, and environmental science, illustrates the exciting nature of the field and enhances the relevancy of the material. Thought-provoking and research-oriented Challenge problems at the end of each chapter in the ebook, based on data from the literature, current topics of interest, and information accessible on the Internet engage students with today s hot topics. 1. The Nature of Analytical Chemistry 2. Chemicals, Apparatus and Unit Operations of Analytical Chemistry 3. Technology Chapter: See your ebook access to Chapter 3 using Spreadsheets in Analaytical Chemistry 4. Calculations Used in Analytical Chemistry 5. Errors in Chemical Analyses 6. Random Errors in Chemical Analysis 7. Technology Chapter: See your ebook to access Chapter 7 Statistical Data Treatment and Evaluation 8. Sampling, Standardization and Calibration 9. Aqueous Solutions and Chemical Equilibria 10. Effect of Electrolytes on Chemical Equilibria 11. Technology Chapter: See your ebook to access Chapter 11 Solving Equilibrium Problems for Complex Systems 12. Gravimetric Methods of Analysis 13. Titrations in Analytical Chemistry 14. Principles of Neutralization Titrations 15. Complex Acid/Base Systems 26

16. Technology Chapter: See your ebook to access Chapter 16 Applications of Neutralization Titrations 17. Complexation and Precipitation Reactions and Titrations 18. Introduction to Electrochemistry 19. Applications of Standard Electrode Potentials 20. Technology Chapter: See your ebook to access Chapter 20 Applications of Oxidation/Reduction Titrations 21. Potentiometry 22. Technology Chapter: See your ebook to access Chapter 22 Bulk Electrolysis: Electrogravitry and Coulometry 23. Voltammetry 24. Introduction to Spectrochemical Methods 25. Technology Chapter: See your ebook to access Chapter 25 Instruments for Optical Spectrometry 26. Molecular Absorption Spectrometry 27. Technology Chapter: See your ebook to access Chapter 27 Molecular Fluorescence Spectroscopy 28. Atomic Spectroscopy 29. Mass Spectroscopy 30. Technology Chapter: See your ebook to access Chapter 30 Kinetic Methods of Analysis 31. Introduction to Analytical Seperations 32. Gas Chromatography 33. High-Performance Liquid Chromatography 34. Technology Chapter: See your ebook to access Chapter Miscellaneous Separation Methods 2014, 784pp, Paperback, 9781408093733 Biochemistry Coming Soon! BIOCHEMISTRY, INTERNATIONAL EDITION, 7E Mary K. Campbell, Mount Holyoke College; Shawn O. Farrell, Colorado State University Introduce your students to the latest developments in biotechnology and genomics with this new edition of Campbell and Farrell s best-selling text for the one-term course. Known for its logical organization, appropriate depth of coverage, and vibrant illustrations, BIOCHEMISTRY, 7e, International Edition, helps your students synthesize the flood of information that has inundated the field since the decoding of the human genome, while showing them how biochemistry principles connect to their everyday lives. The book incorporates up-to-date developments in stem cell research, cloning, and immunology and offers revised coverage of major topics, such as Molecular Biology. Balancing scientific detail with readability, the book is ideal for students studying biochemistry for the first time. For example, in-text questions and problem sets categorized by problem type help students master chemistry and prepare for exams, and Biochemical Connections demonstrate how biochemistry applies to other fields such as health and sports medicine. In addition, the book s revised state-of-the-art visual program improves learning outcomes and its innovative magazine insert, Hot Topics in Biochemistry now reflects the latest advances in the field. Count on BIOCHEMISTRY, 7e, International Edition to lead the way in currency, clarity, and innovation for your onesemester biochemistry course. NEW TO THIS EDITION REVISED COVERAGE OF MOLECULAR BIOLOGY. In this edition, the authors have added new content on Molecular Biology to give students updated and expanded coverage of this key topic. UPDATED MAGAZINE INSERT. The text s innovative magazine insert, Hot Topics in Biochemistry is now updated with the latest advances in the field. REVISED ART PROGRAM. The book s vibrant, state-ofthe art visual program has been revised to even better help students visualize key processes and understand important topics. The visual style and format of the art, a hallmark of the text, is designed to improve student learning outcomes. NEW BIOCHEMICAL CONNECTIONS. Several new Biochemical Connections demonstrate how biochemistry topics relate to the real world in highinterest areas such as allied health, sports medicine, and biotechnology. REORGANIZED END-OF-CHAPTER PROBLEM SETS. The book s exceptionally strong and varied end-ofchapter questions are grouped by question type and include references to section numbers to help students prepare for exams. UPDATED COVERAGE. Each chapter in the text has been updated with the current developments and scientific findings in the biochemistry field. 27

NEW INTEGRATION WITH OWL. For the first time, this best-selling text is available with OWL, the #1 online homework and tutorial system for chemistry. With OWL, you can improve student learning outcomes, while saving time in grading homework and tracking student progress. Developed by chemistry instructors for teaching chemistry, OWL makes homework management a breeze and enables you to address students different learning styles through tutorials, simulations, visualization exercises, and algorithmically-generated homework questions with answer-specific feedback. With OWL s mastery learning approach, students work at their own pace until they understand each concept/skill. Q&A. These student-friendly Q&A features, interspersed throughout the text where questions naturally arise for students, help students learn key biochemistry concepts more efficiently. APPLY YOUR KNOWLEDGE BOXES. Interspersed within chapters, these boxes give students critical problem-solving experience. PROVEN IN-TEXT LEARNING AIDS. Concise summaries and a broad selection of problems and exercises, as well as an annotated bibliography at the close of each chapter, help students review and apply what they ve learned. 1. Biochemistry and the Organization of Cells. 2. Water: The Solvent for Biochemical Reactions. 3. Amino Acids and Peptides. 4. The Three-Dimensional Structure of Proteins. 5. Protein Purification and Characterization Techniques. 6. The Behavior of Proteins: Enzymes. 7. The Behavior of Proteins: Enzymes, Mechanisms, and Control. 8. Lipids and Proteins Are Associated in Biological Membranes. 9. Nucleic Acids: How Structure Conveys Information. 10. Biosynthesis of Nucleic Acids: Replication. 11. Transcription of the Genetic Code: The Biosynthesis of RNA. 12. Protein Synthesis: Translation of the Genetic Message. 13. Nucleic Acid Biotechnology Techniques. 14. Viruses, Cancer and Immunology. 15. The Importance of Energy Changes and Electron Transfer in Metabolism. 16. Carbohydrates. 17. Glycolysis. 18. Storage Mechanisms and Control in Carbohydrate Metabolism. 19. The Citric Acid Cycle. 20. Electron Transport and Oxidative Phosphorylation. 21. Lipid Metabolism. 22. Photosynthesis. 23. The Metabolism of Nitrogen. 24. Integration of Metabolism: Cellular Signaling. 2012, 864pp, Paperback, 9781111425647 Coming Soon! BIOCHEMISTRY, INTERNATIONAL EDITION, 5E Reginald H. Garrett, University of Virginia; Charles M. Grisham, University of Virginia Continuing Garrett and Grisham s innovative conceptual and organizing Essential Questions framework, BIOCHEMISTRY, 5E, International Edition guides students through course concepts in a way that reveals the beauty and usefulness of biochemistry in the everyday world. Offering a balanced and streamlined presentation, this edition has been updated throughout with new material and revised presentations. For the first time, this book is integrated with OWL, a powerful online learning system for chemistry that engages students and improves learning outcomes. NEW TO THIS EDITION Revised Art and Graphics: To increase the pedagogical effectiveness of the art program and to help students better visualize chemical processes, the book s molecular art has been revised to allow for greater consistency in use of atomic color code and now includes more current PyMOL-based molecular graphics. New End-of-Chapter Material: A new Things You Should Know study section has been added to the end-of-chapter material. In addition, new topical headers in the problem sets make it easier to assign problems that pertain to a particular topic. New Coverage: New material has been added on the Ventor Institute s creation of synthetic life; new 28

discussions of protein sectors and metamorphic proteins have been added to Chapter 6; and various free online protein databases have been incorporated throughout the book s narrative. Revised and Updated Coverage: This edition features thoroughly updated coverage of human gene therapy in Chapter 12 and heavily revised coverage of DNA metabolism in Chapter 28. Reorganized Material: Material on reduction potentials and free energy changes in redox reactions has been placed earlier in the book (moved from Chapter 20 to Chapter 3); the discussion of protein techniques was moved from an appendix to Chapter 5 into the chapter proper as an A Deeper Look box; and the DNA Sequencing boxed essay is now expanded and incorporated into the Chapter 11 text narrative. Full Integration with OWL (Online Web Learning): For the first time, this book is fully integrated with OWL, a powerful online learning system for chemistry that engages students, assesses performance, and improves learning outcomes. OWL includes parameterized mastery homework assignments correlated to text sections that encourage students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes an interactive customizable Cengage YouBook (OWL s multimedia e-book). Each chapter in this book is framed around an Essential Question that engages students in the material and encourages curiosity about the subject matter. Human Biochemistry essays emphasize the central role of basic biochemistry in medicine and the health sciences with information on clinically important issues such as diet, diabetes, and cardiovascular health. Critical Developments in Biochemistry essays emphasize recent and historical advances in the field, while A Deeper Look essays expand on the text, highlighting selected topics or experimental observations. End-of-chapter summaries review and briefly answer the key questions posed in each section. Part I: MOLECULAR COMPONENTS OF CELLS. 1. Chemistry is the Logic of Biological Phenomena. 2. Water The Medium of Life. 3. Thermodynamics of Biological Systems. 4. Amino Acids. 5. Proteins: Their Primary Structure and Biological Functions. 6. Proteins: Secondary, Tertiary, and Quaternary Structure. 7. Carbohydrates and Glyco-Conjugates of the Cell Surface. 8. Lipids. 9. Membranes and Membrane Transport. 10. Nucleotides and Nucleic Acids. 11. Structure of Nucleic Acids. 12. Recombinant DNA: Cloning and Creation of Chimeric Genes. Part II: PROTEIN DYNAMICS. 13. Enzyme Kinetics. 14. Mechanisms of Enzyme Action. 15. Enzyme Regulation. 16. Molecular Motors. Part III: METABOLISM AND ITS REGULATION. 17. Nutrition and the Organization of Metabolism. 18. Glycolysis. 19. The Tricarboxylic Acid Cycle. 20. Electron Transport and Oxidative Phosphorylation. 21. Photosynthesis. 22. Gluconeogenesis, Glycogen Metabolism, and the Pentose Phosphate Pathway. 23. Fatty Acid Catabolism. 24. Lipid Biosynthesis. 25. Nitrogen Acquisition and Amino Acid Metabolism. 26. The Synthesis and Degradation of Nucleotides. 27. Metabolic Integration and Organ Specialization. Part IV: INFORMATION TRANSFER. 28. DNA Metabolism. 29. Transcription and the Regulation of Gene Expression. 30. Protein Synthesis. 31. Post-Translational Processing of Proteins and Protein Degradation. 32. The Reception and Transmission of Extracellular Information. 2013, 1280pp, Paperback, 9781133108795 STUDY GUIDE WITH STUDENT SOLUTIONS MANUAL AND PROBLEMS BOOK FOR GARRETT/GRISHAM S BIOCHEMISTRY, 5TH, 5E Reginald H. Garrett, University of Virginia; Charles M. Grisham, University of Virginia This comprehensive combination resource contains 29

chapter summaries, important definitions, illustrations of major metabolic pathways, self-tests, detailed solutions to all end-of-chapter problems, and additional problems with answers. 2013, 608pp, Paperback, 9781133108511 General Chemistry A BEGINNER S GUIDE TO SCIENTIFIC METHOD, INTERNATIONAL EDITION, 4E Stephen S. Carey, Portland Community College This concise yet comprehensive guide provides an introduction to the scientific method of inquiry as well as detailed coverage of the many misapplications of scientific method that define pseudoscience. Compact enough to be used as a supplementary book in a science class, yet thorough enough in its coverage to be used as a core text in a class on scientific method, this text assists students in using the scientific method to design and assess experiments. NEW TO THIS EDITION The explanations have been thoroughly to ensure clarity and readability for the student audience. The discussion of causation in Chapter 3 has been greatly expanded. In Chapter 4, the basic framework for discussing experimental design has been revised to center on false confirmation and rejection. In Chapter 5, the discussion of probability and statistical inference is greatly simplified. Each section now begins with and explains all points in terms of recent causal studies. Two new pseudoscientific fallacies have been added and the text now contains many new and recent illustrations of all the fallacies. Dozens of new exercises and examples have been added to every chapter. End of chapter concept quizzes have been added. An introduction to the scientific method which acknowledges that good science must remain utterly open to revision. Over one hundred practical, relevant exercises and examples address common conceptual issues and pitfalls confronted in students own practices of scientific learning. Real-life examples from scientific literature provide immediate practical applications of the concepts encountered in the book. Preface. 1. SCIENCE. Just What is Science? Asking Why. Scientific Method. The Consequences of Science. Scientific Method in Daily Life. Things to Come. Exercises 2. OBSERVATION. Making Accurate Observations. Anomalous Phenomena. Observing Anomalies. The Burden of Proof. Concept Quiz. Exercises 3. EXPLANATION. Explanation, Theory and Hypothesis. Causation. Correlation. Causal Mechanisms. Underlying Processes. Laws. Function. The Interdependence of Explanatory Methods. Rival Explanations and Ockham s Razor. Explanation and Description. Ultimate Explanations. Concept Quiz. Exercises. 4. EXPERIMENTATION. The Basic Method. Confirmation and Rejection. Designing a Good Test. Real World Experiments. How Not to Design a Test. Conceptual Vagueness. Testing Extraordinary Claims. Predictive Clarity. Bias and Expectation. Concept Quiz. Exercises. 5. ESTABLISHING CAUSAL LINKS. Causal Studies. Ruling Out Chance. Multiple Causal Factors. Randomized, Prospective and Retrospective Studies. Reading Between the Lines. Concept Quiz. Exercises. 6. FALLACIES IN THE NAME OF SCIENCE. What is a Fallacy? False Anomalies. Questionable Arguments by Elimination. Illicit Causal Inferences. Unsupported Analogies and Similarities. Untestable Explanations and Predictions. Empty Jargon. Ad Hoc Rescues. Exploiting Uncertainty. Science and Pseudoscience. Concept Quiz. Exercises. FURTHER READING INDEX 2012, 160pp, Paperback, 9781111726010 30

Coming Soon! CHEMICAL PRINCIPLES, 7E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign This fully updated Seventh Edition of CHEMICAL PRINCIPLES provides a unique organization and a rigorous but understandable introduction to chemistry that emphasizes conceptual understanding and the importance of models. Known for helping students develop a qualitative, conceptual foundation that gets them thinking like chemists, this market-leading text is designed for students with solid mathematical preparation. The Seventh Edition features a new section on Learning to Solve Problems that discusses how to solve problems in a flexible, creative way based on understanding the fundamental ideas of chemistry and asking and answering key questions. The book is also enhanced by new visual problems, new student learning aids, new Chemical Insights boxes, and more. NEW TO THIS EDITION New Co-author: Don DeCoste, brings his wealth of teaching experience to this exceptional Seventh Edition New Learning to Solve Problems Section: A new Section 3.4 emphasizes the importance of conceptual problem solving by showing students how to think their way through a problem. This section discusses how to solve problems in a flexible, creative way based on understanding the fundamental ideas of chemistry and asking and answering key questions. Students will learn that this big picture approach produces more long term, meaningful learning rather than simply memorizing specific steps that are easily forgotten. New Chemical Insights Boxes: Many new and revised Chemical Insights boxes cover such up-to-date topics as geoengineering, laser cooling, graphene, and nanogenerators. New and Revised Problems: Many of the book s end-of-chapter questions and problems have been revised and more than 50 new visual problems have been added. New In-text Learning Aids. A list of Key Terms has been added at the end of each chapter along with an Outline that reviews each chapter. In addition, many of the book s figures have been revised to better serve visual learners. New Cengage YouBook in OWL: An interactive and customizable electronic version of the text--the Cengage YouBook -- features a text edit tool that allows you to modify the textbook narrative as needed. With YouBook, you can quickly re-order entire sections and chapters or hide any content you don t teach to create an ebook that perfectly matches your syllabus. You can further customize the YouBook by publishing web links. Additional media assets may include animated figures, video clips, and more. New Interactive Examples in OWL: Highlighted with an OWL icon in the text, Interactive Examples (key examples from the text transformed into interactive tutorial problems) are now assignable in the OWL program. 1. Chemists and Chemistry. 2. Atoms, Molecules, and Ions. 3. Stoichiometry. 4. Types of Chemical Reactions and Solution Stoichiometry. 5. Gases. 6. Chemical Equilibrium. 7. Acids and Bases. 8. Applications of Aqueous Equilibria. 9. Energy, Enthalpy, and Thermochemistry. 10. Spontaneity, Entropy, and Free Energy. 11. Electrochemistry. 12. Quantum Mechanics and Atomic Theory. 13. Bonding: General Concepts. 14. Covalent Bonding: Orbitals. 15. Chemical Kinetics. 16. Liquids and Solids. 17. Properties of Solutions. 18. The Representative Elements. 19. Transition Metals and Coordination Chemistry. 20. The Nucleus: A Chemist s View. 21. Organic and Biochemical Molecules. Appendix 1. Mathematical Procedures. Appendix 2. Units of Measurement and Conversions Among Units. Appendix 3. Spectral Analysis. Appendix 4. Selected Thermodynamic Data. Appendix 5. Equilibrium Constants and Reduction Potentials. Glossary. Answers to Selected Exercises. 2013, 1200pp, Hardback, 9781111580650 31

CHEMICAL PRINCIPLES IN THE LABORATORY, INTERNATIONAL EDITION, 10E Emil Slowinski, Macalester College; Wayne C. Wolsey, Macalester College; Robert Rossi This Tenth Edition of CHEMICAL PRINCIPLES IN THE LABORATORY, 10e, International Edition maintains the high-quality, time-tested experiments and techniques that have made it a perennial bestseller. Author Wayne Wolsey, with the help of new co-author Rob Rossi, continues to offer complete coverage of basic chemistry principles and present topics in a direct, easy-tounderstand manner. Now, to benefit the environment and reduce the overall cost of the experiments, the new edition features a deepened commitment to green chemistry by reducing the volume and toxicity of experiments as much as possible. NEW TO THIS EDITION GREENER EXPERIMENTS. Four experiments have been made greener by reducing volume and toxicity. This not only benefits the environment, but also reduces the cost of the experiments overall. FLEXIBILITY. You can easily modified labs for use as guided inquiry. Each lab gives students a starting point and the information they need to create and conduct the experiment. EXCEL COVERAGE. A section explains how students can use Excel to simplify making calculations, while an appendix describes how to use Excel software in making calculations in several experiments. A PROVEN APPROACH. The direct approach of this laboratory manual has made it a household name in the General Chemistry laboratory market. Each edition s fully tested experiments are consistently updated to maintain the integrity of this bestselling lab manual. STUDENT-FRIENDLY. Offering complete coverage of basic chemistry principles, this manual presents topics clearly in an easy-to-understand manner, while requiring students to read and demonstrate understanding of the material. ADVANCE STUDY ASSIGNMENTS (ASAs). These assignments include sample questions, usually involving calculations, that are similar to those required in processing the data obtained in each experiment. Students who complete the ASAs prior to coming to lab should have no trouble working up the data they actually observe in the lab session. Experiment 1: The Densities of Liquids and Solids. Experiment 2: Resolution of Matter into Pure Substances, I. Paper Chromatography. Experiment 3: Resolution of Matter into Pure Substances, II. Fractional Crystallization. Experiment 4: Determination of a Chemical Formula. Experiment 5: Identification of a Compound by Mass Relationships. Experiment 6: Properties of Hydrates. Experiment 7: Analysis of an Unknown Chloride. Experiment 8: Verifying the Absolute Zero of Temperature Determination of the Barometric Pressure. Experiment 9: Molar Mass of a Volatile Liquid. Experiment 10: Analysis of an Aluminum-Zinc Alloy. Experiment 11: The Atomic Spectrum of Hydrogen. Experiment 12: The Alkaline Earths and the Halogens Two Families in the Periodic Table. Experiment 13: The Geometrical Structure of Molecules An Experiment Using Molecular Models. Experiment 14: Heat Effects and Calorimetry. Experiment 15: The Vapor Pressure and Heat of Vaporization of a Liquid. Experiment 16: The Structure of Crystals An Experiment Using Models. Experiment 17: Classification of Chemical Substances. Experiment 18: Some Nonmetals and Their Compounds Preparations and Properties. Experiment 19: Molar Mass Determination by Depression of the Freezing Point. Experiment 20: Rates of Chemical Reactions, I. The Iodination of Acetone. Experiment 21: Rates of Chemical Reactions, II. A Clock Reaction. Experiment 22: Properties of Systems in Chemical Equilibrium Le Châtelier s Principle. Experiment 23: Determination of the Equilibrium Constant for a Chemical Reaction. Experiment 24: The Standardization of a Basic Solution and the Determination of the Molar Mass of an Acid. Experiment 25: ph Measurements Buffers and Their Properties. Experiment 26: Determination of the Solubility Product of Ba(IO3)2. Experiment 27: 32

Relative Stabilities of Complex Ions and Precipitates Prepared from Solutions of Copper(II). Experiment 28: Determination of the Hardness of Water. Experiment 29: Synthesis and Analysis of a Coordination Compound. Experiment 30: Determination of Iron by Reaction with Permanganate A Redox Titration. Experiment 31: Determination of an Equivalent Mass by Electrolysis. Experiment 32: Voltaic Cell Measurements. Experiment 33: Preparation of Copper(I) Chloride. Experiment 34: Development of a Scheme for Qualitative Analysis. Experiment 35: Spot Tests for Some Common Anions. Experiment 36: Qualitative Analysis of Group I Cations. Experiment 37: Qualitative Analysis of Group II Cations. Experiment 38: Qualitative Analysis of Group III Cations. Experiment 39: Identification of a Pure Ionic Solid. Experiment 40: The Ten Test Tube Mystery. Experiment 41: Preparation of Aspirin. Experiment 42: Rate Studies on the Decomposition of Aspirin. Experiment 43: Analysis for Vitamin C. Appendix I: Vapor Pressure and Density of Liquid Water. Appendix II: Summary of Solubility Properties of Ions and Solids. Appendix IIA: Some Properties of the Cations in Groups I, II, and III. Appendix III: Table of Atomic Masses (Based on Carbon-12). Appendix IV: Making Measurements Laboratory Techniques. Appendix V: Mathematical Considerations Making Graphs. Appendix VI: Suggested Locker Equipment. Appendix VII: Introduction to Excel. Appendix VIII: Statistical Treatment of Laboratory Data. 2012, 400pp, Spiral, 9781111576608 CHEMISTRY, 7E Principles and Reactions, International Edition William L. Masterton, University of Connecticut, Emeritus; Cecile N. Hurley, University of Connecticut; Edward Neth, University of Connecticut Masterton/Hurley/Neth s CHEMISTRY: PRINCIPLES AND REACTIONS, 7e, International Edition takes students directly to the crux of chemistry s fundamental concepts and allows you to efficiently cover all topics found in the typical general chemistry book. Based on the authors extensive teaching experience, this updated edition includes new concept-driven, rigorous examples, updated examples that focus on molecular reasoning and understanding, and Chemistry: Beyond the Classroom essays that demonstrate the relevance of the concepts and highlight some of the most up-todate uses of chemistry. A strong, enhanced art program assists students in visualizing chemical concepts. Key Concepts correlate to OWL Online Learning, the #1 online homework and tutorial system for chemistry. OWL also includes an interactive ebook for the 7th edition of the textbook and an optional ebook for the Student Study Guide. NEW TO THIS EDITION REORGANIZATION: The authors have reorganized Chapters 13, 15, and 19 to create a better flow from single to multiple equilibria. In addition, Chapters 2-5 have been reorganized to enhance student understanding and mirror the way this material is presented in the classroom. NEW CHAPTER 15: This new chapter covers complex ion and precipitation equilibria to enhance the book s coverage. REVISED VISUALS FOR BETTER CLARITY: Ensure your students understanding of concepts as this edition moves relevant text from captions to talking labels within the art for a clearer presentation of visual images. Contemporary photographs, modern molecular models, and new concept flow charts help further clarify key concepts. NEW AND INNOVATIVE EXAMPLE FORMAT ONE/ TWO COLUMN COMBO: Revised examples provide rigorous practice and opportunities to apply concepts. Each Example begins with a problem statement followed by three problem-solving steps: 1) Analysis (two columns), 2) Strategy (one column), and 3) Solution (two column). This innovative new worked Example format presentation is clear, consistent, and easy to follow. Each example concludes with an End Point, which provides additional insight into the problem. REVISED GRADED AND CONCEPTUAL EXAMPLES: Revised in-text Graded Examples now show the gradual increase in difficulty as problems progress from Step a to Step c. The Graded Examples 33

simulate the presentation of problems on a test. Additional Conceptual Examples lead students through conceptualizing the chemistry principles just discussed and demonstrate how to refine thinking skills at critical points in the chapter. CONNECTION TO FINE ARTS: This edition connects the hard science of chemistry to the humanities and fine arts through chapter openers and literary quotations that enhance each chapter s content. LATEST WORK FROM SPECIALISTS: Guest authors and leaders in specialized fields profile the latest research in Chemistry: Beyond the Classroom boxes. Students see the relevance of concepts in some of the most current work in chemistry, including photochromic and thermochromic materials, coloration biological organisms, molecular structure of rubbery materials, and fuel cells. STRONG COVERAGE OF ORGANIC CHEMISTRY: Students leave your course well equipped with organic chemistry skills through coverage of nomenclature and a greater number of functional groups, as well as coverage of types of organic reactions and material on proteins and carbohydrates. MOLECULAR MODEL ART PROGRAM: Effective models visually reinforce students conceptual understanding. Revised nanoscale views of atoms, molecules, and ions use molecular modeling software and an exacting three-dimensional style to offer effective visual learning tools throughout the text. ABUNDANT IN-TEXT EXAMPLES: More than 115 intext Graded Examples challenge students to solve more difficult material as they proceed through each step of the example. Additional Conceptual Examples lead students through conceptualizing the chemistry principles just discussed before solving the example and encourage higher-order thinking at critical points within the chapter s narrative. 1. Matter and Measurements. 2. Atoms, Molecules, and Ions. 3. Mass Relations in Chemistry; Stoichiometry. 4. Reactions in Aqueous Solution. 5. Gases. 6. Electronic Structure and the Periodic Table. 7. Covalent Bonding. 8. Thermochemistry. 9. Liquids and Solids. 10. Solutions. 11. Rate of Reaction. 12. Gaseous Chemical Equilibrium. 13. Acids and Bases. 14. Equilibria in Acid-Base Solutions. 15. Complex Ion and Precipitation Equilibria 16. Spontaneity of Reaction 17. Electrochemistry. 18. Nuclear Reactions. 19. Complex Ions. 20. Chemistry of the Metals. 21. Chemistry of the Nonmetals. 22. Organic Chemistry. 23. Organic Polymers, Natural and Synthetic. 2012, 800pp, Paperback, 9781111572174 CHEMISTRY, 7E Principles and Reactions, AP* Edition William L. Masterton, University of Connecticut, Emeritus; Cecile N. Hurley, University of Connecticut; Edward Neth, University of Connecticut 2012, 800pp, Hardback, 9781111572587 CHEMISTRY, 3E Principles and Practice, International Edition Daniel L. Reger, University of South Carolina; Scott R. Goode, University of South Carolina; David W. Ball, Cleveland State University A text that truly embodies its name, CHEMISTRY: PRINCIPLES AND PRACTICE, 3rd, International Edition connects the chemistry students learn in the classroom (principles) with real-world uses of chemistry (practice). The authors accomplish this by starting each chapter with an application drawn from a chemical field of interest and revisiting that application throughout 34

the chapter. The Case Studies, Practice of Chemistry essays, and Ethics in Chemistry questions reinforce the connection of chemistry topics to areas such as forensics, organic chemistry, biochemistry, and industry. NEW TO THIS EDITION Each chapter begins with an opening application drawn from a chemical field of interest, which is revisited throughout the chapter. Worked Examples include problem flow diagrams that map out the problem-solving process in a graphical manner, aiding students in developing problemsolving thought processes and strategies. Many examples use color to aid students in showing how the initial data in the problem is transformed through the various steps of the problem to the answer. Case Studies are multi-pronged, multi-step problems that examine real world uses of chemistry. Summary Problems focus on a problem of chemical interest and draw on material from the entire chapter for their solutions. Ethics in Chemistry questions, located at the end of each chapter before the problem sets, emphasize the human side of chemistry and remind students that chemistry is not just a set of facts. These questions discuss the ethical issues and dilemmas scientists face in practicing their profession. They also are good exercises for schools that have a writing-across-thecurriculum requirement. This edition fully integrates OWL (Online Web-based Learning), the homework management system trusted by tens of thousands of students. Integrated end-of-chapter questions correlate to OWL. An optional e-book of this edition is also available in OWL. In addition, Go Chemistry learning modules developed by award-winning chemists offer mini-lectures and learning tools that play on video ipods, personal video players, QuickTime, Windows Media Player, and itunes. (ipods, itunes, iphone are products of Apple, Inc.) This book presents chemistry concepts in an experimental context by demonstrating how the facts and theories have come from many years of experimentation. This is emphasized in the text with margin icons. Each section begins with a set of Learning Objectives and ends with an Objectives Review. The exercises also are grouped by objectives. Principles of Chemistry essays expand and/or reinforce important topics discussed in the book. Practice of Chemistry essays are real-world applications of chemistry; i.e., why and how chemists and other professionals use chemistry in their jobs and daily lives. The text includes approximately 2000 Questions and Exercises. Questions are qualitative in nature, often conceptual, and include problem-solving skills. Questions that are suitable for a brief writing exercise are designated with the symbol of a pencil. The morechallenging items are designated with a triangle. The text also has end-of-chapter exercises available for use in OWL, Brooks/Cole s online homework and assessment system. Exercises are paired, with the odd-numbered ones having answers in the appendix and a similar even-numbered problem immediately following. While most exercises appear in the order in which they are discussed, there are also Chapter Exercises that are uncategorized, and Cumulative Exercises that integrate concepts and methods introduced in earlier chapters. Cumulative Exercises often contain multiple parts and/or multiple steps. 1. Introduction to Chemistry. 2. Atoms, Molecules, and Ions. 3. Equations, the Mole, and Chemical Formulas. 5. Chemical Reactions in Solution Thermochemistry. 6. The Gaseous State. 7. Electronic Structure. 8. The Periodic Table: Structure and Trends. 9. Chemical Bonds. 10. Molecular Structure and Bonding Theories. 11. Liquids and Solids. 12. Solutions. 13. Chemical Kinetics. 14. Chemical Equilibrium. 15. Solutions of Acids and Bases. 16. Reactions Between Acids and Bases. 17. Chemical Thermodynamics. 18. Electrochemistry. 19. Metals, Coordination Chemistry, and Metallurgy. 20. The Chemistry of Hydrogen, Elements in Groups 3A through 6A, and the Noble Gases. 21. Nuclear Chemistry. 22. Organic Chemistry and Biochemistry. Appendix A: Math Procedures. Appendix B: Selected Physical Constants. Appendix C: Unit Conversion Factors. Appendix D: Names of Ions. Appendix E: Properties of Water. Appendix F: Solubility Products, Acids, and Bases. Appendix G: Thermodynamic Constants for Selected Compounds. Appendix H: Standard Reduction 35

Potentials at 25. Appendix I: Glossary. Appendix J: Answers to Selected Exercises. 2010, 1120pp, Paperback, 9780495559832 CHEMISTRY, 4E The Molecular Science, International Edition John W. Moore, University of Wisconsin, Madison; Conrad L. Stanitski, Franklin and Marshall College; Peter C. Jurs, Pennsylvania State University Your students will be engaged in the active study of chemistry with CHEMISTRY: THE MOLECULAR SCIENCE, 4e, Internatinoal Edition. Authors Moore, Stanitski, and Jurs infuse their text with timely applications that reveal chemistry as a lively and relevant subject that is fundamental to a broad range of disciplines such as engineering, biology, and environmental science. The Fourth Edition features an enhanced problem-solving methodology, a complete revision of its award-winning art program to even better help students visualize chemical processes at a molecular level, integrated coverage of organic and biochemistry content, and full media integration with OWL Online Web Learning and Go Chemistry. New content, more visualization problems, updated applications in a wide range of disciplines, and unique new end-of-chapter grid questions based on awardwinning chemistry education research have been added throughout the text. In addition, many of the book s end-of-chapter questions are accompanied by interactive, assignable, online lessons in OWL the #1 online learning system for chemistry. NEW TO THIS EDITION A COMPLETELY REVISED ART PROGRAM. Nearly all the art in the book s award-winning art program was critically reviewed, then revised to better help students ability to visualize molecular-scale processes and connect these processes to real-world phenomena. AN ENHANCED FOCUS ON PROBLEM SOLVING. In addition to an overall emphasis on the step-by-step process, the book now has a new focus on solving real problems and includes more end-of-chapter problems and unique new grid problems based on chemical education research. The authors move students away from merely memorizing algorithmic solutions by including thought-provoking exercises linked to conceptual understanding. MORE END-OF-CHAPTER PROBLEMS IN OWL. Most end-of-chapter questions are now coded into the OWL system and parameterized, giving students the opportunity to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. GO CHEMISTRY MINI-VIDEO LECTURES. Go Chemistry portable lecture videos are referenced throughout the text, encouraging students to study on the go with their ipod, smart phone, or other media player. NEW AND REVISED BOXED. The authors have updated their proven pedagogical features: Chemistry You Can Do, Estimation, Portrait of a Scientist, and Tools of Chemistry. Almost all Chemistry in the News features are entirely new. EMPHASIS ON THREE CONCEPTUAL LEVELS OF CHEMISTRY. The authors emphasize the Macroscopic (laboratory or real-world phenomena), Nanoscale (particles: atoms, molecules, and ions), and Symbolic (chemical formulas and equations) conceptual levels of chemistry throughout the text. PROBLEM-SOLVING FOCUS. The authors proven problem-solving methodology, introduced in Chapter 1 and consistently used throughout the book, features worked-out Problem-Solving Examples that use a five-part structure: Question (problem), Answer, Strategy and Explanation (which outlines a step-bystep approach to solving the problem), Reasonable Answer Check, and Problem-Solving Practice that provides a similar question or questions, with answers in an appendix. Many exercises are specifically designed to allow students to test their conceptual 36

understanding. ESTIMATION BOXES. Many chapters include boxes that pose a problem for which a rough calculation suffices. These boxes help students learn various means of approximation and further develop reasonableness of answer skills that are useful for calculator-less exams such as the MCAT. A WEALTH OF EXAMPLES, PRACTICE PROBLEMS, AND EXERCISES. Designed to stimulate active thinking, encourage student participation, and refine understanding of concepts the book includes more examples, practice problems and exercises than are found in most similar textbooks 1. The Nature of Chemistry. 2. Atoms and Elements. 3. Chemical Compounds. 4. Quantities of Reactants and Products. 5. Chemical Reactions. 6. Energy and Chemical Reactions. 7. Electron Configurations and the Periodic Table. 8. Covalent Bonding. 9. Molecular Structures. 10. Gases and the Atmosphere. 11. Liquids, Solids, and Materials. 12. Fuels, Organic Chemicals, and Polymers. 13. Chemical Kinetics: Rates of Reactions. 14. Chemical Equilibrium. 15. The Chemistry of Solutes and Solutions. 16. Acids and Bases. 17. Additional Aqueous Equilibria. 18. Thermodynamics: Directionality of Chemical Reactions. 19. Electrochemistry and Its Applications. 20. Nuclear Chemistry. 21. The Chemistry of the Main Group Elements. 22. Chemistry of Selected Transition Elements and Coordination Compounds. 2011, 1264pp, Paperback, 9781439049662 CHEMISTRY An Atoms First Approach, International Edition Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Steve and Susan Zumdahl s texts focus on helping students build critical thinking skills through the process of becoming independent problem-solvers. They help students learn to think like a chemists so they can apply the problem solving process to all aspects of their lives. In CHEMISTRY: AN ATOMS FIRST APPROACH, 1e, International Edition the Zumdahls use a meaningful approach that begins with the atom and proceeds through the concept of molecules, structure, and bonding, to more complex materials and their properties. Because this approach differs from what most students have experienced in high school courses, it encourages them to focus on conceptual learning early in the course, rather than relying on memorization and a plug and chug method of problem solving that even the best students can fall back on when confronted with familiar material. The atoms first organization provides an opportunity for students to use the tools of critical thinkers: to ask questions, to apply rules and models and to AN ATOMS FIRST APPROACH. By taking an atoms first approach, the authors are able to provide students with a unified story built around an organizing principle start the course with smallest element, the atom, and build from there. Building their explanations around this structure, the authors consistently show the importance and relevance of studying chemistry. A FOCUS ON CONCEPTUAL UNDERSTANDING. Rather than focusing on memorizing, the book gives students the tools they need to become critical thinkers: to ask questions, to apply rules and develop models, and to evaluate the outcome. A LOGICAL ORGANIZATION. Chapter 1 provides an introduction to the key components of the story the atom, atomic structure, energy, and the mole. Chapter 2 initiates the plan of going from the simple to the complex. Chapter 3 covers counting by weighing, atomic masses, the mole, and introduces chemical equations. Chapter 4 covers the fundamental ideas of bonding to explain how atoms are tied together. Chapter 5 covers detailed models of bonding and structure: Chapter 6 covers chemical energy; Chapters 7 and 8 cover gases, liquids, and solids, and Chapter 9 covers stoichiometry. A STRONG PROBLEM-SOLVING ORIENTATION. 37

Throughout the text, problem-solving strategies help students learn to solve problems by thinking them through rather than brute-force memorizing. Section 6.2 Learning to Solve Problems emphasizes the importance of thoughtful, creative problem solving, demonstrating that thinking through a problem produces more long-term, meaningful learning that can be applied to real life than memorizing steps that apply only to a particular type of problem. The problem-solving process is organized in terms of Where are we going? ; How do we get there? and Reality Check, which prompts students to check whether their answer makes sense. STUDENT-ORIENTED LEARNING AIDS. Problemsolving strategy boxes help students focus on particular aspects of problem-solving; concept summary boxes help students organize their thinking about crucial concepts; and chemical connections boxes present applications of chemistry in various fields and in daily life. INTERACTIVE EXAMPLES encourage students to think their way through the example instead of passively reading through the solution. Electronic versions of select examples are assignable in OWL. Students can work these Interactive Examples multiple times to help them master the problem-solving process, receiving slightly different examples each time they attempt an Interactive Example. END-OF-CHAPTER VISUAL EXERCISES, called out with an icon, provide students with opportunities to demonstrate a conceptual understanding of fundamental chemical principles. Many take an atomic view of matter to help students appreciate the usefulness of the atomic model in understanding macroscopic properties. Other problems ask students to interpret graphs or to explain figures. A FOCUS ON THE FUNDAMENTAL IDEAS OF CHEMISTRY. Numerous discussions, illustrations, and exercises are designed to help students overcome misconceptions by providing a more accurate picture of the fundamental ideas of chemistry. The book emphasizes the importance of developing a qualitative understanding of concepts before approaching quantitative problems. AN OUTSTANDING ART PROGRAM. The book represents the microscopic world of chemistry to give students a picture in their minds of what the atoms and molecules are doing through an excellent art program and animations. END-OF-CHAPTER ACTIVE LEARNING QUESTIONS. Because students often learn the most when they teach each other, these questions are intended for group discussion. Review Chapter: Measurement and Calculations in Chemistry. 1. Chemical Foundations. 2. Atomic Structure and Periodicity. 3. Atoms to Molecules. 4. Bonding: General Concepts. 5. Molecular Structure and Orbitals. 6. Chemical Energy. 7. Gases. 8. Liquids and Solids. 9. Stoichiometry. 10. Types of Chemical Reactions and Solution Stoichiometry. 11. Properties of Solutions. 12. Chemical Kinetics. 13. Chemical Equilibrium. 14. Acids and Bases. 15. Acid-Base Equilibria. 16. Solubility and Complex Ion Equilibria. 17. Spontaneity, Entropy, and Free Energy. 18. Electrochemistry. 19. The Nucleus: A Chemist s View. 20. The Representative Elements. 21. Transition Metals and coordination Chemistry. 22. Organic and Biological Molecules. Appendix 1: SI Units and Conversion Factors. Appendix 2: Mathematical Procedures. Appendix 3: The Quantitative Kinetic Molecular Model. Appendix 4: Spectral Analysis. Appendix 5: Selected Thermodynamic Data. Appendix 6: Equilibrium Constants and Reduction Potentials. 2012, 1152pp, Paperback, 9780840065865 CHEMISTRY & CHEMICAL REACTIVITY, AP* EDITION, 8E John C. Kotz, State University of New York, Oneonta; Paul M. Treichel, University of Wisconsin, Madison; John Townsend, West Chester University of Pennsylvania 2012, 1312pp, Hardback, 9781111427047 38

CHEMISTRY 2012 UPDATE, AP* EDITION, 8E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign 2012, 1232pp, Hardback, 9781111577346 CHEMISTRY AND CHEMICAL REACTIVITY, INTERNATIONAL EDITION, 8E John C. Kotz, State University of New York, Oneonta; Paul M. Treichel, University of Wisconsin, Madison; John Townsend, West Chester University of Pennsylvania Providing the most innovative homework, assessment, and study tools available for general chemistry, this thoroughly revised new edition of CHEMISTRY & CHEMICAL REACTIVITY, 8e, International Edition continues to offer the signature clear explanations, macro to micro orientation, enhanced problem-solving strategies, and superior art program that have made it a best-seller. The text emphasizes the visual nature of chemistry, illustrating the close interrelationship of the macroscopic, symbolic, and particulate levels of chemistry. The highly acclaimed art program illustrates each of these levels in engaging detail and is fully integrated with key media components. Now featuring more coverage of green/sustainable chemistry, the new edition provides students with even more problem-solving support through a revised format for worked problems, new problem strategy maps, new Review & Check problems, and more. OWL (Online Web Learning), a fully customizable homework and tutorial system (now featuring an interactive e-book) maximizes student study time and your options for assignments. Quality writing, seamless technology integration, and a rich ancillary package remain the hallmarks of CHEMISTRY & CHEMICAL REACTIVITY, 8e, International Edition. NEW TO THIS EDITION REVISED WORKED EXAMPLES. Through the text s new six-part worked example structure, students learn how to approach a problem rather than to memorize problem types and solution approaches. Worked example headers use the following structure: 1) A Problem statement; 2) A What Do You Know? section that asks students to assess what they already know about solving the problem; 3) A Strategy for approaching the problem; 4) A fully worked Solution; 5) A Think About Your Answer section, and 6) A Check Your Understanding section that prompts students to check whether their answer makes sense. NEW PROBLEM STRATEGY MAPS. Selected worked examples have new Strategy Maps that give students a visual view of the complete problem-solving strategy. New Video Strategy Solutions are integrated into this edition s new interactive ebook. MORE COVERAGE OF GREEN/SUSTAINABLE CHEMISTRY. A green chemistry expert reviewed the entire book, and based on this review, the authors worked much more green/sustainable chemistry into the book. NEW REVIEW & CHECK PROBLEMS. These sectionending problems help students hone their skill in assessing whether they understand the concepts in the section. ENHANCED ART PROGRAM. The art program has been revised to make concepts easier to understand. In addition, a new graph style helps students understand graphical information. VISUAL TOOLS. With the text s extensive use of molecular representations, your students can move beyond plugging numbers into an equation to a true 39

understanding of what s going on at the molecular level. The authors consistently depict molecules in chemical equations and use unique space-filling molecular art that more completely tie the text s molecular art to problem solving and media. CASE STUDY BOXES. Cases show students where chemistry has been used to solve a problem or where chemistry is important in everyday matters. Examples include the use of isotopes to catch athletes who cheat using illegal drugs, a washing machine that injects silver into the wash, acryalmide in French fries, a comparison of ethanol and gasoline, and the amount of salt in seawater. Questions posed in each Case Study are answered in an appendix. IN THE LABORATORY QUESTIONS. These end-ofchapter questions address techniques used and work performed in the general chemistry laboratory to help students make the connection between lecture topics and lab work. INTERCHAPTERS. Insightful Interchapters on biochemistry, modern materials, environmental chemistry, and the chemistry of energy sources address topics in a brief but visually exciting way. This format allows these topics to be easily integrated into the course or skipped without interrupting the narrative. BEYOND THE EXAM. The text correlates Chapter Goals with Study Questions to help students develop a conceptual understanding of chemistry and a skill in problem-solving that will serve them long after their final exams. Part I: THE BASIC TOOLS OF CHEMISTRY. 1. Basic Concepts of Chemistry. Let s Review: The Tools of Quantitative Chemistry. 2. Atoms, Molecules, and Ions. 3. Chemical Reactions. 4. Stoichiometry: Quantitative Information About Chemical Reactions. 5. Principles of Chemical Reactivity: Energy and Chemical Reactions. Interchapter: The Chemistry of Fuels and Energy Sources. PART II: THE STRUCTURE ATOMS AND MOLECULES. 6. The Structure of Atoms. 7. The Structure of Atoms and Periodic Trends. Interchapter: Milestones in the Development of Chemistry and the Modern View of Atoms and Molecules. 8. Bonding and Molecular Structure. 9. Bonding and Molecular Structure: Orbital Hybridization and Molecular Orbitals. 10. Carbon: Not Just Another Element Interchapter: The Chemistry of Life: Biochemistry. PART III: STATES OF MATTER. 11. Gases and Their Properties. 12. Intermolecular Forces and Liquids. 13. The Chemistry of Solids. 14. Solutions and Their Behavior. Interchapter: The Chemistry of Modern Materials. PART IV: THE CONTROL OF CHEMICAL REACTIONS. 15. Chemical Kinetics: The Rates of Chemical Reactions. 16. Principles of Chemical Reactivity: Equilibria. 17. Principles of Chemical Reactivity: The Chemistry of Acids and Bases. 18. Principles of Reactivity: Other Aspects of Aqueous Equilibria. 19. Principles of Reactivity: Entropy and Free Energy. 20. Principles of Reactivity: Electron Transfer Reactions. Interchapter: The Chemistry of the Environment. PART V: THE CHEMISTRY OF THE ELEMENTS AND THEIR COMPOUNDS. 21. The Chemistry of the Main Group Elements. 22. The Chemistry of the Transition Elements. 23. Nuclear Chemistry. Appendix A: Using Logarithms and the Quadratic Equation. Appendix B: Some Important Physical Concepts. Appendix C: Abbreviations and Useful Conversion Factors. Appendix D: Physical Constants. Appendix E: A Brief Guide to Naming Organic Compounds. Appendix F: Values for the Ionization Energies and Electron Attachment Enthalpies of the Elements. Appendix G: Vapor Pressure of Water at Various Temperatures. Appendix H: Ionization Constants for Aqueous Weak Acids at 25ºC. Appendix I: Ionization Constants for Aqueous Weak Bases at 25ºC. Appendix J: Solubility Product Constants for Some Inorganic Compounds at 25ºC. Appendix K: Formation Constants for Some Complex Ions in Aqueous Solution at 25ºC. Appendix L: Selected Thermodynamic Values. Appendix M: Standard Reduction Potentials in Aqueous Solution at 25ºC. Appendix N: Answers to Chapter Opening Questions and Case Study Questions. Appendix O: Answers to Check Your Understanding Questions Appendix P: Answers to Review & Check Questions Appendix Q: Answers to Selected Interchapter Study Questions. Appendix R: Answers to Selected Study Questions. 2012, 1296pp, Paperback, 9781111427023 40

CHEMISTRY FOR ENGINEERING STUDENTS, INTERNATIONAL EDITION, 2E Larry Brown, Texas A&M University; Tom Holme, Iowa State University Enhanced with a remarkable number of new problems and applications, the Second Edition of CHEMISTRY FOR ENGINEERS, International Edition provides a concise, thorough, and relevant introduction to chemistry that prepares students for further study in any engineering field. Updated with even more questions and applications specifically geared toward engineering students, the book emphasizes the connection between molecular properties and observable physical properties and the connections between chemistry and other subjects studied by engineering students, such as mathematics and physics. This new edition is now fully supported by OWL, the most widely-used online learning system for chemistry. NEW TO THIS EDITION Updated Insight Into boxes focusing on topics such as nanomaterials (Ch. 1), green chemistry in the development and cleanup of explosives (Ch. 3), biomaterials (Ch. 7), and weathering in concrete (Ch. 12) reflect new trends and innovations in chemistry and show connections between chemistry concepts and engineering applications. Additional problems related to engineering applications have been added to every chapter. Selected end-of-chapter problems (approximately 30%) are now available in OWL: Online Web Learning system. Insights Into boxes lead off each chapter with engineering applications, that raise questions that are answered later in the chapter, show connections between chemistry concepts and engineering applications, and are supported by end-of-chapter problems. Focus on Problem Solving sections at the end of each chapter support the book s problem-solving emphasis through a mix of multi-step quantitative and qualitative questions that require students to think outside the context of the information given and focus on the process of finding a solution to a problem, not the solution itself. MathConnections boxes offer mathematical review at point of use, expanding and reviewing math concepts as they pertain to the particular topic being studied. Detailed Example Problems illustrate good problemsolving practices by focusing on the reasoning of the solution as well as the calculations. Strategy sections first offer a way to solve the problem, then reinforce the solution with Analyze Your Answer sections (which walk students through a double check of their answers), then allow students to practice the skill with Check Your Understanding exercises. A chapter summary and key terms (which include the section number where each term first appears) conclude each chapter to help students review and study for tests. 1. Introduction to Chemistry. 2. Atoms and Molecules. 3. Molecules, Moles, & Chemical Equations. 4. Stoichiometry. 5. Gases. 6. The Periodic Table and Atomic Structure. 7. Chemical Bonding and Molecular Structure. 8. Molecules and Materials. 9. Energy and Chemistry. 10. Entropy and the Second Law of Thermodynamics. 11. Chemical Kinetics. 12. Chemical Equilibrium. 13. Electrochemistry. 14. Nuclear Chemistry (Available through Custom Publishing). Appendices. 2011, 608pp, Paperback, 9780538733649 41

CHEMISTRY FOR MATRICULATION Azilah Abd Rahman, University of Malaya; Aishah Mohamed Jelan, University of Malaya; Mazdida Sulaiman, University of Malaya Suitable for Matriculation, STPM and Pre-U courses Large set of worked-out examples An extensive collection of questions at the end of chapter Four-colored illustration with explanations to ease understanding Prepared by a group of experienced academicians Foreword Preface About the Authors Brief Contents Contents Chap 1 Matter and Measurement Chap 2 Atoms and Elements Chap 3 Molecules, Ions, and Their Components Chap 4 Chemical Equations and Stoichiometry Chap 5 Reactions in Aqueous Solution Chap 6 Principles of Reactivity: Energy and Chemical Reactions Chap 7 Atomic Structure Chap 8 Atomic Electron Configurations and Chemical Periodicity Chap 9 Bonding and Molecular Structure: Fundamental Concepts Chap 10 Bonding and Molecular Structure: Orbital Hybridization and Molecular Orbitals Chap 11 Gases and Their Properties Chap 12 Intermolecular Forces, Liquids, and Solids Chap 13 Solutions and Their Behavior Chap 14 Principles of Reactivity: Chemical Kinetics Chap 15 Principles of Reactivity: Chemical Equilibria Chap 16 Principles of Reactivity: Chemistry of Acids and Bases Chap 17 Principles of Reactivity: Other Aspects of Aqueous Equilibria Chap 18 Principles of Reactivity: Electron Transfer Reactions Appendices Index 2006, 656pp, 9789812544247 CHEMISTRY WITH CB COURSESMART EBOOK, 9E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign CB CourseSmart ebook The ultimate ebook experience has arrived! Easily access our ebooks with features that will improve your reading experience, and tools to help you take notes and organize your studies. This fully updated Ninth Edition of Steven and Susan Zumdahl s CHEMISTRY brings together the solid pedagogy, easy-to-use media, and interactive exercises that today s instructors need for their general chemistry course. Rather than focusing on rote memorization, CHEMISTRY uses a thoughtful approach built on problem-solving. For the Ninth Edition, the authors have added a new emphasis on critical systematic problem solving, new critical thinking questions, and new computer-based interactive examples to help students learn how to approach and solve chemical problems--to learn to think like chemists--so that they can apply the process of problem solving to all aspects of their lives. Students are provided with the tools to become critical thinkers: to ask questions, to apply rules and develop models, and to evaluate the outcome. In addition, Steven and Susan Zumdahl crafted ChemWork, an online program included in OWL Online Web Learning to support their approach, much as an instructor would offer support during office hours. ChemWork is just one of many study aids available with CHEMISTRY that supports the hallmarks of the textbook--a strong emphasis on models, real world applications, visual learning, and independent problem solving. A NEW EMPHASIS ON SYSTEMATIC PROBLEM SOLVING now appears in the applications of 42

dimensional analysis. NEW CRITICAL THINKING QUESTIONS have been added throughout the text to emphasize the importance of conceptual learning. NEW COMPUTER-BASED INTERACTIVE EXAMPLES force students to think through the example stepby-step rather than simply scan the written example in the text as many students do. New Interactive Examples are available in OWL Online Web Learning. In addition, key examples from the text have been made into Interactive Tutorial problems and are available to assign in the OWL program. NEW CHEMWORK PROBLEMS have been added to the end-of-chapter problems throughout the text to test students understanding of core concepts. They can be worked as pencil-and-paper problems or in interactive form in OWL, where students who solve a problem with no assistance can proceed directly to the answer and students who need help can get assistance through a series of hints. The hints in OWL--usually in the form of interactive questions that guide students through the problem-solving process--are modeled after the way an instructor would assist a student with homework problems during office hours. Students cannot derive the answer in OWL through pattern recognition; rather, they are encouraged to continue working though the hints to arrive at the answer. NEW END-OF CHAPTER QUESTIONS AND PROBLEMS have been added throughout the text. THE REVISED AND UPDATED ART PROGRAM has been modified as needed, and new macro/micro illustrations have been added. A NEW SECTION ON LIMITING REACTANTS in Chapter 3, the treatment of stoichiometry, emphasizes calculating the amounts of products that can be obtained from each reactant. Students are taught how to select a limiting reactant both by comparing the amounts of reactants present and by calculating the amounts of products that can be formed by complete consumption of each reactant. A NEW SECTION ON PHOTOELECTRON SPECTROSCOPY was added to Chapter 9 (Section 9.6). ENHANCED OWL (ONLINE WEB LEARNING) INTEGRATION: For the Ninth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes Student Self- Assessments, ChemWork problems, Interactive Examples from the text, the interactive customizable Cengage YouBook, a customizable ipad-compatible multimedia ebook, and an optional Solutions Manual ebook. PROBLEM-SOLVING STRATEGY BOXES focus the student s attention on the very important process of problem solving, helping them learn to think like chemists. 1. Chemical Foundations. 2. Atoms, Molecules, and Ions. 3. Stoichiometry. 4. Types of Chemical Reactions and Solution Stoichiometry. 5. Gases 6. Thermochemistry. 7. Atomic Structure and Periodicity. 8. Bonding: General Concepts. 9. Covalent Bonding: Orbitals. 10. Liquids and Solids. 11. Properties of Solutions. 12. Chemical Kinetics. 13. Chemical Equilibrium. 14. Acids and Bases. 15. Acid-Base Equilibria. 16. Solubility and Complex Ion Equilibria. 17. Spontaneity, Entropy, and Free Energy. 18. Electrochemistry. 19. The Nucleus: A Chemist s View. 20. The Representative Elements. 21. Transition Metals and Coordination Chemistry. 22. Organic and Biological Molecules. Appendix 1. Mathematical Procedures. A1.1 Exponential Notation. A1.2 Logarithms. A1.3 Graphing Functions. A1.4 Solving Quadratic Equations. A1.5 Uncertainties in Measurements. Appendix 2. The Quantitative Kinetic Molecular Model. Appendix 3. Spectral Analysis. Appendix 4. Selected Thermodynamic Data. Appendix 5. Equilibrium Constants and Reduction Potentials. A5.1 Values of Ka for Some Common Monoprotic Acids. A5.2 Stepwise Dissociation Constants for Several Common Polyprotic Acids. A5.3 Values of Kb for Some Common Weak Bases. A5.4 Ksp Values at 25_C for Common Ionic Solids. A5.5 Standard Reduction Potentials at 25_C (298K) for Many Common Half- Reactions. Appendix 6. SI Units and Conversion Factors. Glossary. Answers to Selected Exercises. 2014, 752pp, Paperback, 9789814568715 43

Coming Soon! CHEMISTRY, INTERNATIONAL EDITION, 10E Kenneth W. Whitten, University of Georgia; Raymond E. Davis, University of Texas, Austin; Larry Peck, Texas A&M University; George G. Stanley, Louisiana State University This new edition of CHEMISTRY, 10E, International Edition continues to incorporate a strong molecular reasoning focus, amplified problem-solving exercises, a wide range of real-life examples and applications, and innovative technological resources. With this text s focus on molecular reasoning, your students will learn to think at the molecular level and make connections between molecular structure and macroscopic properties. The Tenth Edition has been revised throughout and now includes a reorganization of the descriptive chemistry chapters to improve the flow of topics, a new basic math skills Appendix, an updated art program with new talking labels that fully explain what is going on in the figure, and much more. NEW TO THIS EDITION REORGANIZATION OF DESCRIPTIVE CHEMISTRY CHAPTERS (22-28): To facilitate an improved flow of the descriptive chemistry topics optionally covered in many courses and to provide more convenient options for custom versions of the textbook, Chapters 22 through 28 have been reorganized as follows: Chapter 22 is now Nuclear Chemistry; Chapter 23, Organic Chemistry I: Formulas, Names and Properties; Chapter 24, Organic Chemistry II: Shapes, Selected Reactions, and Biopolymers; Chapter 25, Coordination Compounds; Chapter 26, Metals I: Metallurgy; Chapter 27, Metals II: Properties and Reactions; and Chapter 28, Some Nonmetals and Metalloids. NEW BASIC MATH SKILLS APPENDIX: To aid the flow of introductory chemistry material in Chapter 1, a review of topics in basic mathematics skills, including scientific notation and use of significant figures, with numerous Examples, now appears in Appendix A. Related Exercises remain in the Measurements and Calculations area at the end of Chapter 1. REORGANIZED INTRODUCTION TO AQUEOUS SOLUTIONS: Section 6-1 has been reorganized to improve the descriptive introduction to aspects of aqueous solutions, including ionization and dissociation, acids, bases, and solubility guidelines. These basic ideas are then elaborated in the classification of reactions in the remainder of Chapter 6 and serve as a foundation throughout the textbook for further discussion of physical and chemical properties of solutions. MORE COMPREHENSIVE COVERAGE OF CENTRAL ATOM LONE PAIRS: In Chapter 8, a more comprehensive tabular summary of the influence of central atom lone pairs on molecular geometry has been added to enhance student understanding. A REVISED AND UPDATED ART PROGRAM: The Tenth Edition s art program has been revised to include talking labels placed strategically within figures to explain what is going on in the illustration, so students can focus on learning instead of trying to figure out what is going on by going back and forth between a caption and the art. To exemplify the beauty and excitement of chemistry, the individual layouts of many figures have been revised to be more visually pleasing, balanced, and organized. The art program now includes more molecular models generated by the latest software to enhance the molecular reasoning theme. All electrostatic charge potential (ECP) art includes a more thorough explanation of its use. ENHANCED OWL ONLINE WEB LEARNING: For the Tenth Edition, OWL now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes the Cengage YouBook, a customizable ipad-compatible multimedia ebook, Quick Prep assignments that help students learn skills essential for success in General Chemistry, and an optional solutions manual ebook. MOLECULAR REASONING AND VISUALIZATION 44

EMPHASIS: Molecular reasoning is woven throughout the text in chapter objectives, chapter essays, examples, and end-of-chapter problems and highlighted by a molecular reasoning icon. CHAPTER-OPENING APPLICATIONS AND CHEMISTRY IN USE BOXES: These built-in learning aids illustrate the practical applications of chemistry in such areas as the environment, the development of science, research and technology, and our daily lives. BEYOND THE TEXTBOOK QUESTIONS: These endof-chapter questions ask students to solve problems through the use of online exercises in OWL, as well as other materials. STOP & THINK BOXES: Throughout the text, these boxes alert students to common mistakes and points of emphasis in problem solving. 1. The Foundations of Chemistry. 2. Chemical Formulas and Composition Stoichiometry. 3. Chemical Equations and Reaction Stoichiometry. 4. The Structure of Atoms. 5. Chemical Periodicity. 6. Some Types of Chemical Reactions. 7. Chemical Bonding. 8. Molecular Structure and Covalent Bonding Theories. 9. Molecular Orbitals in Chemical Bonding. 10. Reactions in Aqueous Solutions I: Acids, Bases, and Salts. 11. Reactions in Aqueous Solutions II: Calculations. 12. Gases and the Kinetic- Molecular Theory. 13. Liquids and Solids. 14. Solutions. 15. Chemical Thermodynamics. 16. Chemical Kinetics. 17. Chemical Equilibrium. 18. Ionic Equilibria I: Acids and Bases. 19. Ionic Equilibria II: Buffers and Titration Curves. 20. Ionic Equilibria III: The Solubility Product Principle. 21. Electrochemistry. 22. Nuclear Chemistry. 23. Organic Chemistry I: Formulas, Names and Properties. 24. Organic Chemistry II: Shapes, selected Reactions, and Biopolymers. 25. Coordination Compounds. 26. Metals I: Metallurgy. 27. Metals II: Properties and Reactions. 28. Some Nonmetals and Metalloids. Appendix A: Basic Math Skills (includes new significant figure section). Appendix B: Electron Configurations of the Atoms of the Elements. Appendix C: Common Units, Equivalences, and Conversion Factors. Appendix D: Physical Constants. Appendix E: Some Physical Constants for a Few Common Substances. Appendix F: Ionization Constants for Weak Acids at 25 C. Appendix G: Ionization Constants for Weak Bases at 25 C. Appendix H: Solubility Product Constants for Some Inorganic Compounds at 25 C. Appendix I: Dissociation Constants for Some Complex Ions. Appendix J: Standard Reduction Potentials in Aqueous Solution at 25 C. Appendix K: Selected Thermodynamic Values at 298.15 K. Appendix L: Answers to Selected Even-Numbered Numerical Exercises. Index of Equations. Glossary/ Index. 2014, 1184pp, Paperback, 9781133933595 ESSENTIAL ALGEBRA FOR CHEMISTRY STUDENTS, 2E David W. Ball, Cleveland State University Available free when packaged with any Cengage textbook or available separately for a minimal cost at www.cengagebrain.com, this short book is designed to help you build confidence and competency in the essential mathematics skills necessary to survive in general chemistry. Each chapter focuses on a specific type of skill and has worked-out examples to show how these skills translate to chemical problem solving. NEW TO THIS EDITION REFERENCES TO OWL: This edition includes references to OWL material, which is being incorporated into all of Brooks/Cole s GOB and general chemistry texts. These online algebra skills exercises serve as additional practice of some of the skills in the book. EXTENSIVELY EDITED AND REVISED: We have edited and revised this text to underscore the basic skills students need for algebra in chemistry. Numerous examples and exercises, with answers, as well as problems specifically designed for use with calculators. This book is adaptable because it is not text-specific; however, the ordering of chapters mimics the order of 45

how much of the material is covered in introductory courses. The initial chapters serve as a useful baseline algebra review for all beginning chemistry students, with later chapters covering skills that are more specific to particular types of quantitative chemical problem solving. Preface. 1. Numbers, Units, and Scientific Notation. 2. Arithmetic Evaluation. 3. Significant Figures. 4. Converting Units. 5. Using Chemical Reactions to Make Conversion Factors. 6. Using Mathematical Formulas. 7. Advanced Math Topics. 8. Making Graphs. Index. 2006, 192pp, Paperback, 9780495013273 EXPERIMENTS IN GENERAL CHEMISTRY, 6E Steven L. Murov, Modesto Junior College EXPERIMENTS IN GENERAL CHEMISTRY, Sixth Edition, has been designed to stimulate curiosity and insight, and to clearly connect lecture and laboratory concepts and techniques. To accomplish this goal, an extensive effort has been made to develop experiments that maximize a discovery-oriented approach and minimize personal hazards and ecological impact. Like earlier editions, the use of chromates, barium, lead, mercury, and nickel salts has been avoided. The absence of these hazardous substances should minimize disposal problems and costs. This lab manual focuses not only on what happens during chemical reactions, but also helps students understand why chemical reactions occur. The sequence of experiments has been refined to follow topics covered in most general chemistry textbooks. In addition, Murov has included a correlation chart that links the experiments in the manual to the corresponding chapter topics in several Cengage Learning general chemistry titles. Each experiment- -framed by pre-and post-laboratory exercises and concluding thought-provoking questions--helps to enhance students conceptual understanding. NEW TO THIS EDITION Labs have been updated with the most recent data and values in order to accurately reflect the changes in lab courses. The new Activity 35 adds additional challenges and experiments, and Activity 36 provides exercises that develop graphing skills. Murov focuses not only on what happens during chemical reactions but also helps students understand why chemical reactions occur. Each experiment includes pre-laboratory exercises and thought-provoking questions (with answers to selected questions). Review Exercises, found at the end of the manual, help students test their understanding of key concepts and synthesize the material they have learned. A number of experiments include post-laboratory exercises and conclude with a set of review exercises. A procedure for following the visual clock reaction spectroscopically, instead of visually, is included in the kinetics experiment. This also provides a link between the equilibrium and kinetics experiments. As with the previous editions, the use of chromates, barium, lead, mercury, and nickel salts has been avoided, effectively minimizing disposal problems and decreasing costs. A correlation chart links the experiments to corresponding chapter topics in several Cengage Learning general chemistry titles, including Kotz, Masterton, Moore, and Whitten. An Online Instructor s Manual contains resources designed to streamline and maximize the effectiveness of course preparation. It includes a list of chemicals and quantities required for each experiment per student and solutions to Pre-Lab problems. Preface, Correlation table and Chemistry Resources SAFETY FIRST 1. Early Explorations and Terminology. 2. Separation of Mixtures. 3. Measurements and Identification Techniques. 4. Density, Accuracy, Precision 46

and Graphing. 5. Empirical Formulas. 6. Classification of Chemical Reactions. 7. Quantitative Precipitation. 8. Electrical Conductivity and Electrolytes. 9. Ionic Reactions. 10. Activities of Metals. 11. Quantitative Solution Chemistry. 12. Thermochemistry. 13. Properties of Elements and Compounds: An Internet Study. 14. Spectroscopy of Cobalt (II) Ion. 15. Lewis Structures and Molecular Models. 16. Molecular Polarity and Chromatography. 17. Gas Law Studies. 18. Cooling Curves and Crystal Structures. 19. Water Purification and Analysis. 20. Organic Models and Isomerism. 21. Acids and Bases: Reactions and Standardization. 22. Acids and Bases: Analysis. 23. Acids and Bases: ph, pka Measurements. 24. Equilibrium - Solubility Product. 25. Equilibrium - Determination of Keq. 26. Complexes. 27. Rates and Mechanisms of Reactions - Visual and/ or Spectroscopic Monitoring. 28. Synthesis of Copper (II) Glycinate. 29. Standardization of Thiosulfate. 30. Analysis of Bleach and Copper (II) Glycinate. 31. Redox Reactions. 32. Electrochemistry. 33. Spectroscopic Analysis of Aspirin. 34. Polymer Properties and Selections 35. Additional Challenges and Experiments 36. Graphing Quantitative Relationships Appendix 1: Properties of Substances Appendix 2: Common Ions by Charge Appendix 3: Solubilities of Ionic Compounds Appendix 4: Solutions to Starred Prelaboratory Problems 2015, 464pp, Paperback, 9781285458540 EXPERIMENTS IN GENERAL CHEMISTRY, 5E Steven L. Murov, Modesto Junior College EXPERIMENTS IN GENERAL CHEMISTRY is the perfect textbook to prepared you for success in a chemistry class. This innovative book is not only full of exciting experiments but will help you understand the chemistry behind what is happening. With this guide in your pocket, acing any chemistry class will be a breeze! NEW TO THIS EDITION Experiment 5, Empirical Formulas, in addition to the determination of the empirical formula of a hydrate, now also contains the synthesis and empirical formula determination of zinc iodide. The internet study of the properties of elements and compounds in Experiment 13, Properties of Elements and Compounds: An Internet Study, now includes new material on nuclear stability and less duplication of material directly covered in textbooks. Experiment 12, Thermochemistry, and Experiment 35, Polymers, Material Selection using the Internet and Some Fun, now have additional internet exercises. The correlation chart has been updated to link the experiments to the corresponding chapter topics in several Brooks/Cole general chemistry titles, including Kotz, Masterton, Moore, and Whitten. Carefully revised to reinforce the connections made between experiments, the Fifth Edition enhances students conceptual understanding of key principles and emphasizes how each lab adds to the sum of the students chemical experience. SAFETY FIRST. 1. Early Explorations and Terminology. 2. Separation of Mixtures. 3. Measurements and Identification Techniques. 4. Density, Accuracy, Precision and Graphing. 5. Empirical Formulas. 6. Classification of Chemical Reactions. 7. Quantitative Precipitation. 8. Electrical Conductivity and Electrolytes. 9. Ionic Reactions. 10. Activities of Metals. 11. Quantitative Solution Chemistry. 12. Thermochemistry. 13. Properties of Elements and Compounds: An Internet Study. 14. Spectroscopy of Cobalt (II) Ion. 15. Lewis Structures and Molecular Models. 16. Molecular Polarity and Chromatography. 17. Gas Law Studies. 18. Cooling Curves and Crystal Structures. 19. Water Purification and Analysis. 20. Organic Models and Isomerism. 21. Acids and Bases: Reactions and Standardization. 22. Acids and Bases: Analysis. 23. Acids and Bases: ph, pka Measurements. 24. Acids and Bases: Carbonate Analysis. 25. Equilibrium - Solubility Product. 26. Equilibrium - Determination of Keq. 27. Complexes. 28. Rates and Mechanisms of Reactions - Visual and/or Spectroscopic Monitoring. 29. Synthesis of Copper (II) Glycinate. 30. 47

Standardization of Thiosulfate. 31. Analysis of Bleach and Copper (II) Glycinate. 32. Redox Reactions. 33. Electrochemistry. 34. Spectroscopic Analysis of Aspirin. 35. Polymers, Material Selection using the Internet and Some Fun. Review Exercises. Appendixes. 2007, 464pp, Paperback, 9780495125389 EXPERIMENTS IN GENERAL CHEMISTRY, LAB MANUAL, 10E Rupert Wentworth, Indiana University; Barbara H. Munk Each experiment in this manual was selected to match topics in the textbook and includes an introduction, a procedure, a page of pre-lab exercises about the concepts the lab illustrates, and a report form. Some have a scenario that places the experiment in a realworld context. In addition, each experiment has a link to a set of references and helpful online resources. 2013, 512pp, Paperback, 9781111989422 EXPERIMENTS IN GENERAL CHEMISTRY: INQUIRY AND SKILL BUILDING, 2E Vickie Williamson, Texas A&M University; Larry Peck, Texas A&M University With many years of teaching experience in the classroom and laboratory, Vickie Williamson and Larry Peck have created EXPERIMENTS IN GENERAL CHEMISTRY: INQUIRY AND SKILL BUILDING, 2nd edition with carefully crafted and tested experiments designed to complement any general chemistry curriculum. The authors have selected three types of lab experiments to meet all of the needs of students and instructors looking for a selection of laboratory pedagogy. There are Skill Building experiments to develop techniques and demonstrate previously developed concepts, Guided Inquiry experiments to direct the students to collect data on variables without previously studying the concepts and guide them to look for patterns in the data, and Open Inquiry experiments to allow the students to apply concepts or relationships in a new setting. Twenty-eight experiments feature Pre-Lab questions and Post-Lab questions on perforated pages for easy removal of worksheets, and there is a Common Procedures and Concepts section as an appendix for easy retrieval of basic information for students. NEW TO THIS EDITION Updated experiments throughout with 2 brand new experiments added to this edition. Two-semester safety agreements. Perforated pages allow for easy removal of worksheets. Thirty total experiments (2 completely new) featuring Skill Building experiments, Guided Inquiry experiments and Open Inquiry experiments, meet all of the needs of students and instructors looking for a selection of laboratory pedagogy. Common Procedures and Concepts section allows for easy retrieval of basic information for students. EXPERIMENT 1 - Are Labels Accurate or Precise? (An Open Inquiry Experiment). EXPERIMENT 2 - Density Measurements (A Skill Building Experiment). EXPERIMENT 3 - Cost of a Chemical Product(A Guided Inquiry Experiment). EXPERIMENT 4 - Soap Making (A Skill Building Experiment). EXPERIMENT 5 - Reactions of Calcium(A Guided Inquiry Experiment). EXPERIMENT 6 - Aluminum and Copper (II) Chloride(A Guided Inquiry Experiment). EXPERIMENT 7 (was 6) - Recycling Aluminum Cans (A Skill Building Experiment). EXPERIMENT 8 - Patterns(A Guided 48

Inquiry Experiment). EXPERIMENT 9 (was 7) - Solutions and Crystals of Alum (A Guided Inquiry Experiment). EXPERIMENT 10 (was 8) - Analysis of a Carbonated Beverage(A Guided Inquiry Experiment). EXPERIMENT 11 (was 9) - Mass Relationships in Reactions(An Open Inquiry Experiment). EXPERIMENT 12 (was 10) - Shapes of Molecules and Ions(A Guided Inquiry Experiment). EXPERIMENT 13 (was 11) - The Fuel in a Bic Lighter(A Guided Inquiry Experiment). EXPERIMENT 14 (was 12) - Alka-Seltzer : An Application of Gas Laws(A Guided Inquiry Experiment). EXPERIMENT 15 (was 13) - Freezing Points of Solutions(A Guided Inquiry Experiment). EXPERIMENT 16 (was 14) - Spectrochemical Analysis(A Guided Inquiry Experiment). EXPERIMENT 17 (was 15) - Heat of Crystallization(A Skill Building Experiment). EXPERIMENT 18 (was 16) - Enthalpy of Reaction (A Guided Inquiry Experiment). EXPERIMENT 19 (was 17) - The Kinetics of the Decomposition of Hydrogen Peroxide(A Guided Inquiry Experiment). EXPERIMENT 20 (was 18) - Kinetics of Decoloration of Crystal Violet(A Guided Inquiry Experiment). EXPERIMENT 21 (was 19) - Factors Affecting Reactions(A Guided Inquiry Experiment). EXPERIMENT 22 (was 20) - Formation of a Complex(A Skill Building Experiment). EXPERIMENT 23 (was 21) - Acids and ph(a Guided Inquiry Experiment). EXPERIMENT 24 (was 22) - Reactions of Acids And Bases(A Guided Inquiry Experiment). EXPERIMENT 25 (was 23) - Acids and Bases(An Open Inquiry Experiment). EXPERIMENT 26 (was 24) - Electrochemistry(A Guided Inquiry Experiment). EXPERIMENT 27 (was 25) - Small- Scale Redox Titration(A Skill Building Experiment). EXPERIMENT 28 (was 26) - The Copper Cycle(A Open Inquiry Experiment). EXPERIMENT 29 (was 27) - Organic Molecules(A Guided Inquiry Experiment). EXPERIMENT 30 (was 28) - Reactions of Organic Compounds(A Guided Inquiry Experiment). Common Procedures and Concepts. 2014, 412pp, Paperback, 9781285433172 Coming Soon! GENERAL CHEMISTRY, INTERNATIONAL EDITION, 10E Darrell D. Ebbing, Wayne State University; Steven D. Gammon, Western Washington University The tenth edition of this market-leading text has been substantially revised to meet the rapidly changing instructional demands of GENERAL CHEMISTRY, International Edition professors. Known for its carefully developed, thoroughly integrated, step-by-step approach to problem solving, GENERAL CHEMISTRY, International Edition helps students master quantitative skills and build a lasting conceptual understanding of key chemical concepts. The tenth edition retains this hallmark approach and builds upon the conceptual focus through key new features and revisions. NEW TO THIS EDITION Beautiful new book design that is user friendly, but also conveys the sense of excitement surrounding chemistry that the author team wants students to see! Heavily revised art and photography program that helps highlight the excitement of chemistry while explaining key concepts. New talking labels have been added to the art and photos. These talk students through the figure and explain what they are seeing- -what they need to know. A new pedagogical feature has been added to all of the examples that are woven throughout the book. The new feature in the examples is called the Gaining Mastery Toolbox. Every tool box contains Critical Concepts and Solution Essentials. Critical Concepts are concepts from the relevant chapter that the student needs to know in order to work through the example. The Solution Essential segment features a list of information needed to solve the problem presented--for example, a student may need the periodic table, Avogadro s number, etc. 49

Many new and revised end-of-chapter problems and questions including a new type of strategy problem. TWO TIER questions are ones that ask a student a question and then they must choose the answer. The second tier question is where they choose why they chose that answer. Students often choose the correct answer but not the correct reason they answered it correctly, which reveals that they do not under the concept being demonstrated New end of chapter Check List for Review feature- -this new feature is presented in an easy-to-follow tabular format that includes a summary of facts and concepts, learning objectives, important terms, and key equations. This innovative presentation is organized by section. Up-to-date coverage in every chapter of the latest changes in chemistry. Beautiful new book design that is user friendly, but also conveys the sense of excitement surrounding chemistry that the author team wants students to see! Heavily revised art and photography program that helps highlight the excitement of chemistry while explaining key concepts. New talking labels have been added to the art and photos. These talk students through the figure and explain what they are seeing- -what they need to know. new pedagogical feature has been added to all of the examples that are woven throughout the book. The new feature in the examples is called the Gaining Mastery Toolbox. Every tool box contains Critical Concepts and Solution Essentials. Critical Concepts are concepts from the relevant chapter that the student needs to know in order to work through the example. The Solution Essential segment features a list of information needed to solve the problem presented--for example, a student may need the periodic table, Avogadro s number, etc. 1. Chemistry and Measurement. 2. Atoms, Molecules, and Ions. 3. Calculations with Chemical Formulas and Equations. 4. Chemical Reactions. 5. The Gaseous State. 6. Thermochemistry. 7. Quantum Theory of the Atom. 8. Electron Configurations and Periodicity. 9. Ionic and Covalent Bonding. 10. Molecular Geometry and Chemical Bonding Theory. 11. States of Matter; Liquids and Solids. 12. Solutions. 13. Rates of Reaction. 14. Chemical Equilibrium. 15. Acids and Bases. 16. Acid-Base Equilibria. 17. Solubility and Complex-Ion Equilibria. 18. Thermodynamics and Equilibrium. 19. Electrochemistry. 20. Nuclear Chemistry. 21. Chemistry of the Main-Group Elements. 22. The Transition Elements and Coordination Compounds. 23. Organic Chemistry. 24. Polymer Materials: Synthetic and Biological. 2013, 1152pp, Paperback, 9781111989491 GUIDED EXPLORATIONS IN GENERAL CHEMISTRY, 2E David Hanson This student workbook is designed to support Process Oriented Guided Inquiry Learning (POGIL) with activities that promote a student-focused active classroom. It is an excellent accompaniment to CHEMISTRY: THE MOLECULAR SCIENCE or any other general chemistry text. NEW TO THIS EDITION The 2nd edition features a reorganized TOC that reflects the majority of General Chemistry texts. Nine special problem topics for students have been recognized and given 5 extra practice problems that can be done in the classroom or assigned as homework. An answer key is provided on the Instructor s companion site. A new To the Instructor section has been added to the Preface to compliment the To the Student section from the 1st edition. 1. The Nature of Matter. 2. Scientists Love to Measure. 3. The Nuclear Atom. 4. The Mole and Molar Mass. 5. Naming Compounds. 6. Determining Molecular Formulas. 7. Reaction Stoichiometry. 8. Limiting 50

Reactants. 9. Types of Chemical Reactions 10. Solution Concentration and Stoichiometry. 11. Energy. 12. Enthalpy. 13. Fuels. 14. Photoelectron Spectrum of Argon. 15. Periodic Trends in Properties of Elements. 16. Lewis Structures. 17. Electronegativity and Bond Properties. 18. VSEPR Model. 19. Hybrid Atomic Orbitals. 20. Gases and the Ideal Gas Law. 21. Partial Pressures. 22. Phases of Matter. 23. Phase Diagrams. 24. Solubility. 25. Colligative Properties. 26. Rates of Chemical Reactions. 27. Reaction Mechanisms. 28. Equilibrium Constant and Reaction Quotient. 29. Calculating Equilibrium Concentrations. 30. Acid Ionization Constants. 31. Calculations Involving Acid Ionization Constants. 32. Buffers. 33. Acid Base Titrations. 34. Entropy. 35. Free Energy. 36. Electrochemical Cells. 37. Electrolytic Cells. 38. Radioactivity. 39. Rates of Nuclear Decay. 40. Chemistry of Main Group Elements. 41. Electronic Structure and Properties. 42. Transition metals and Coordination Compounds. 43. Magnetism and Color in Coordination Compounds. 44. Organic Functional Groups. 2011, 224pp, Paperback, 9781439049655 INQUIRY BASED LEARNING GUIDE FOR ZUMDAHL/ZUMDAHL S CHEMISTRY, 9TH, 9E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign 2014, 96pp, Spiral, 9781133611523 LAB EXPERIMENTS FOR GENERAL CHEMISTRY, 5E Toby F. Block, Georgia Institute of Technology; George M. McKelvy, Georgia Institute of Technology This is not your average chemistry lab manual. LAB EXPERIMENTS FOR GENERAL CHEMISTRY walks you through the standard chemistry experiments but it also includes guided discovery experiments that let you take control of your own learning. With this manual, you won t get lost in class and you might just learn something new as well. Get the grade you need and experiment for yourself with LAB EXPERIMENTS FOR GENERAL CHEMISTRY. NEW TO THIS EDITION The Fifth Edition features three new experiments; Using the Right Container, in the Right Manner, VSEPR, and Getting the End Point to Approximate the Equivalence Point. The Fifth Edition suggests options for conducting some experiments with CBL-2 technology. Instructions for using spreadsheets in graphing are provided for each experiment. Expanded directions on calculations are provided for some experiments, where they are needed. The experiments in this lab manual are extremely flexible and will work with a variety of books and curricula. Every chapter begins with objectives and procedures in a nutshell so that students are directed to focus on the significance of the experiments without getting lost in the procedures. Every experiment includes safety cautions, first aid, and disposal methods for using chemicals in a lab. Report sheets are included to help students clarify 51

calculations of their experiments. Data tables are updated and easy to read in order to facilitate teaching and learning. Students are given an introduction to the use of spreadsheets in presenting graphical data and preparing reports. 1. Using the Right Container, in the Right Manner. 2. On the Nature of Pennies. 3. Density. 4. VSEPR. 5. Separation of a Mixture into Its Components by Fractional Crystallization. 6. Fun with Solutions. 7. Properties of Oxides, Hydroxides and Oxo-Acids. 8. Volumetric Analysis: Acid/Base Titration Using Indicators. 9. Job s Method: Determining the Stoichiometry of a Reaction. 10. The Synthesis of Cobalt Oxalate Hydrate. 11. The Synthesis of a Nitrite Complex. 12. Determination of the Composition of Cobalt Oxalate Hydrate. 13. The Gasimetric Analysis of a Nitrite Complex. 14. The Burning of a Candle. 15. The Vapor Pressure of Water. 16. Freezing- Point Depression. 17. Absorption Spectroscopy and Beer s Law. 18. Getting the End Point to Approximate the Equivalence Point. 19. Determination of the Dissociation Constant of an Acid/Base Indicator. 20. Temperature Change and Equilibrium. 21. Analysis of Bleach for Hypochlorite Content. 22. Electrochemical Cells. 23. Enthalpy of Hydration of Ammonium Chloride. 24. Thermodynamic Prediction of Precipitation Reactions. 25. Kinetic Study of the Reaction between Iron (III) Ions and Iodide Ions. 26. Qualitative Analysis of Household Chemicals. 27. Analysis of a Soluble Salt. Appendices. 2006, 512pp, Paperback, 9780534424480 LAB MANUAL FOR ZUMDAHL/ ZUMDAHL S CHEMISTRY, 9TH, 9E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Build skill and confidence in the lab with the 61 experiments included in this manual. Safety is strongly emphasized throughout the lab manual. 2014, 624pp, Paperback, 9781133611486 LABORATORY INQUIRY IN CHEMISTRY, 3E Richard Bauer, Arizona State University; James Birk, Arizona State University; Doug Sawyer, Scottsdale Community College LABORATORY INQUIRY IN CHEMISTRY, Thrid Edition provides a unique set of guided-inquiry investigations that focus on constructing knowledge about the conceptual basis of laboratory techniques, instead of simply learning techniques. By focusing on developing skills for designing experiments, solving problems, thinking critically, and selecting and applying appropriate techniques, the authors expose students to a realistic laboratory experience, typical of the practicing chemist. This new edition continues the proven three-phase learning cycle: exploration of chemical behaviors within the context of the problems posed; concept invention--the use of data and observations to construct accepted scientific knowledge about the concepts explored in the laboratory investigation; and, concept application- -where students apply their conceptual understanding of the investigation at hand by modifying or extending the experiments, and write a report that emphasizes conceptual relevance. These college and honors level inquiry-based experiments correlate well with the recommended experiments outlined by the Advanced Placement Chemistry Development Committee. NEW TO THIS EDITION The following new experiments have been added to this editon:5. What Relationships Exist Among 52

Elements?11. How Much Acetic Acid Is in Vinegar?24. Why Do Liquids Evaporate at Different Rates?In addition, new photos have been added throughout to better demonstrate lab instruments, procedures and techniques. Proven three-phase learning cycle: exploration of chemical behaviors within the context of the problems posed; concept invention--the use of data and observations to construct accepted scientific knowledge about the concepts explored in the laboratory investigation; and concept application-- where students apply their conceptual understanding of the investigation at hand by modifying or extending the experiments, and write a report that emphasizes conceptual relevance. The Investigations. 1. What Are the Safety Concerns in the Laboratory? 2. Whats in the Flask? 3. How Should Data Trends Be Presented? 4. How Is Lab Equipment Used? 5. What Relationships Exist Among Elements? 6. What s in the Bottles? 7. How Can the Waste Be Made Useful? 8. Is the Water Hard or Soft? 9. How Hot Is the Water? 10. Which Metal Will Burn the Skin? 11. How Much Acetic Acid Is in Vinegar? 12. Are All Neutralization Reactions the Same? 13. How Many Waters of Hydration Are in the Formula? 14. How Much Sodium Bicarbonate Is in the Mixture? 15. Is It Economical to Recycle Aluminum? 16. What Is a Copper Cycle? 17. Who Wrote the Ransom Note? 18. How Can UV Sensitive Beads Be Used to Test Sunscreens? 19. What Factors Affect the Intensity of Color? 20. How Much Cobalt Is in the Soil? 21. How Much Copper Is in the Coin? 22. Which Iron Compound Is It? 23. Should We Mine This Ore? 24. Why Do Liquids Evaporate at Different Rates? 25. What Are the Structures of Some Alloys? 26. How Is LED Light Color Related to Composition? 27. What Is the Molar Mass of Mars Ice Gas? 28. How Much Gas Is Produced? 29. Which Alcohols Are in the Barrels? 30. How Is Heat of Combustion Measured Indirectly? 31. What Is the Rate Law? 32. How Fast Does the Crystal Violet Decolorize? 33. Why Is the Vinegar Factory Rusting? 34. What Factors Affect the Solubility of Kidney Stones? 35. How Many Chemicals Are in the Vial? 36. What Factors Affect Chemical Equilibrium? 37. What Is the Formation Constant? 38. Are Household Items Acidic, Basic, or Neutral? 39. What Is the ph of Soil? 40. What Is the Acid Dissociation Constant? 41. What Is the Solubility Product? 42. What Are Some Chemical Properties of Cream of Tartar? 43. What Are the Metals? 44. How Can a Battery Be Made from Coins? 45. What Is the Complex Ion? 46. What Formulation Makes the Best Toy? 47. How Are Anions Identified? 48. How Are Cations Identified? 49. How Are More Cations Identified? 50. How Are Ionic Solids Identified? Appendix A: Automated Data Collection. Appendix B: Transmittance and Absorbance Data Collection. Appendix C: Measuring ph. Appendix D: Temperature Data Collection. Appendix E: Pressure Data Collection. Appendix F: Voltage Data Collection. Appendix G: Selected Laboratory Techniques. Appendix H: Laboratory Equipment. Appendix I: Sample Material Safety Data Sheet. Appendix J: Tables 2009, 288pp, Paperback, 9780495113454 MICROSCALE EXPERIMENTS FOR GENERAL CHEMISTRY Kenneth L. Williamson, Mount Holyoke College, Emeritus; John Little, St. Mary s High School This lab manual for general chemistry courses provides superior microscale experiments that can also help departments meet the growing problems of cost and disposal. A Cleaning-Up feature also teaches students about waste disposal and hazardous waste. 1. Observing a Chemical Reaction 2. Densities of Organic Liquids 3. Separation of a Mixture 4. Crystallization 5. Sublimation 6. Solubility and Solutions 7. Isolation of the Silver in a Dime 8. Synthesis of Manganese (II) Chloride 9. Analysis of Copper Oxide 10. Gravimetric Determination of Chloride Ion Concentration 11. Gravimetric Determination of Sulfate Ion Content 12. 53

Carbonate or Bicarbonate? 13. Hydrates: Structure and Properties 14. Periodic Trends in Physical Properties: Densities of Unknowns 15. Distillation 16. Avogadros Law 17. Charles Law: Temperature/Volume Relationships for Gases 18. Determination of the Molar Volume of a Gas and the Universal Gas Constant 19. Oxidation- Reduction Reactions 20. Analysis by Oxidation- Reduction Titration 21. Concentration of Hydrogen Peroxide 22. The Oxidation State of Nitrogen 23. Micro- Electrolysis of a Salt 24. Calorimetry: Heat of Fusion of Ice, Heat of Neutralization, Specific Heat of a Metal, Heat of Solution 25. Thermodynamics of Oxidation of Acetone by Hypochlorite 26. Reaction Kinetics: The Aldol Condensation of Acetone with Benzaldehyde 27. Metal Reactivities The Activity Series for Metals 28. Nonmetal Reactivities The Activity Series for Nonmetals 29. Synthesis and Analysis of an Iron Compound 30. Partition Coefficient of an Organic Acid 31. Gas Chemistry: Sulfur Dioxide 32. Gas Chemistry: Ammonia 33. Gas Chemistry: Carbon Dioxide 34. Determination of Molar Mass by Vapor Density The Dumas Method of Molecular Weight Determination 35. Solubility, Complex Ions, and Qualitative Analysis 36. Water Softening 37. Growing Crystals in Gels 38. Synthesis and Analysis of Aspirin 39. Synthesis of Esters 40. Oxidation-Reduction Dyeing with Indigo, The Blue Jeans Dye 41. Synthesis of Slime Large set of worked-out examples An extensive collection of questions at the end of chapter Solutions for selected questions at the end of chapter Four-colored illustration with explanations to ease understanding Prepared by a group of experienced academicians Foreword Preface About the Authors Brief Contents Contents Chap 1 Introduction to organic Chemistry Chap 2 Alkanes and Cycloalkanes Chap 3 Alkenes Chap 4 Alkynes Chap 5 Haloalkanes Chap 6 Alcohols Chap 7 Benzene and its Derivatives Chap 8 Carbonyl Compounds Chap 9 Carboxylic Acids Chap 10 Functional Derivatives of Carboxylic Acids Chap 11 Amines Chap 12 Amino Acids and Proteins Chap 13 Carbohydrates Chap 14 Organic Polymer Chemistry Answer Appendix 1 Appendix 2 Appendix 3 Appendix 4 Appendix 5 Appendix 6 Appendix 7 Index 2006, 615pp, Paperback, 9789812654243 1997, 400pp, Paperback, 9780669416060 PRINCIPLES OF CHEMISTRY The Molecular Science, International Edition John W. Moore, University of Wisconsin, Madison; Conrad L. Stanitski, Franklin and Marshall College; Peter C. Jurs, Pennsylvania State University ORGANIC CHEMISTRY FOR MATRICULATION Mohd. Hilmi Jaafar, University of Malaya; Lim You Sie, University of Malaya Suitable for Matriculation, STPM and Pre-U courses PRINCIPLES OF CHEMISTRY: THE MOLECULAR SCIENCE, INTERNATIONAL EDITION offers a rigorous and complete general chemistry textbook in a briefer format. This book offers students all the topics covered in the typical general course and tested on the American Chemical Society exams at the same depth and rigor as the longer books but at an easier-to-use size and a more agreeable price. Problem-Solving Examples, Estimation boxes, visual aids, and study tools appear throughout 54

to ensure that students master difficult material and are well prepared for class. Problem-Solving Examples. Problem-Solving Examples appear throughout the text to ensure that students learn to effectively use problem-solving strategies. Estimation Boxes. Estimation boxes in each chapter help students improve their approximation skills. Visual Aids. Instructive macro/nano art helps students visualize difficult concepts. In-text Learning Aids. Questions for Review and Thought, in-text Exercises, and In Closing lists ensure that students understand recently introduced concepts and help them to prepare for class. Problem-Solving Examples. Problem-Solving Examples throughout the text help you master problem-solving strategies. Why Care About Chemistry? Cleaning Drinking Water. How Science is Done. Identifying Matter: Physical Properties. Chemical Change and Chemical Properties. Classifying Matter: Substances and Mixtures. Classifying Matter: Elements and Compounds. Nanoscale Theories and Models. The Atomic Theory. The Chemical Elements. Communicating Chemistry: Symbolism. Modern Chemical Sciences. 2. ATOMS AND ELEMENTS. Atomic Structure and Subatomic Particles. The Nuclear Atom. The Sizes of Atoms and the Units Used to Represent Them. Uncertainty and Significant Figures. Atomic Numbers and Mass Numbers. Isotopes and Atomic Weight. Amounts of Substances: The Mole. Molar Mass and Problem Solving. The Periodic Table. 3. CHEMICAL COMPOUNDS. Molecular Compounds. Naming Binary Inorganic Compounds. Hydrocarbons. Alkanes and Their Isomers. Ions and Ionic Compounds. Naming Ions and Ionic Compounds. Bonding in and Properties of Ionic Compounds. Moles of Compounds. Percent Composition. Determining Empirical and Molecular Formulas. The Biological Periodic Table. 4. QUANTITIES OF REACTANTS AND PRODUCTS. Chemical Equations. Patterns of Chemical Reactions. Balancing Chemical Equations. The Mole and Chemical Reactions: The Macro-Nano Connection. Reactions with One Reactant in Limited Supply. Evaluating the Success of a Synthesis: Percent Yield. Percent Composition and Empirical Formulas. 5. CHEMICAL REACTIONS. Exchange Reactions: Precipitation and Net Ionic Equations. Acids, Bases, and Acid-Base Exchange Reactions. Oxidation- Reduction Reactions. Oxidation Numbers and Redox Reactions. Displacement Reactions, Redox, and the Activity Series. Solution Concentration. Molarity and Reactions in Aqueous Solutions. Aqueous Solution Titrations. 6. ENERGY AND CHEMICAL REACTIONS. The Nature of Energy. Conservation of Energy. Heat Capacity. Energy and Enthalpy. Thermochemical Expressions. Enthalpy Changes for Chemical Reactions. Where Does the Energy Come From? Measuring Enthalpy Changes: Calorimetry. Hess s Law. Standard Molar Enthalpies of Formation. 7. ELECTRON CONFIGURATIONS AND THE PERIODIC TABLE. Electromagnetic Radiation and Matter. Planck s Quantum Theory. The Bohr Model of the Hydrogen Atom. Beyond the Bohr Model: The Quantum Mechanical Model of the Atom. Quantum Numbers, Energy Levels, and Atomic Orbitals. Shapes of Atomic Orbitals. Atom Electron Configurations. Ion Electron Configurations. Periodic Trends: Atomic Radii. Periodic Trends: Ionic Radii. Periodic Trends: Ionization Energies. Periodic Trends: Electron Affinities. Energy Considerations in Ionic Compound Formation. 8. COVALENT BONDING. Covalent Bonding. Single Covalent Bonds and Lewis Structures. Multiple Covalent Bonds. Multiple Covalent Bonds in Hydrocarbons. Bond Properties: Bond Length and Bond Energy. Bond Properties: Bond Polarity and Electronegativity. Formal Charge. Lewis Structures and Resonance. Exceptions to the Octet Rule. Molecular Orbital Theory. 9. MOLECULAR STRUCTURE. Using Molecular Models. Predicting Molecular Shapes: VSEPR. Orbitals Consistent with Molecular Shapes: Hybridization. Hybridization in Molecules with Multiple Bonds. Molecular Polarity. Noncovalent Interactions and Forces Between Molecules. 10. GASES AND THE ATMOSPHERE. The Atmosphere. Gase Pressure. Kinetic-Molecular Theory. The Behavior of Ideal Gases. Quantities of Gases in Chemical Reactions. Gas Density and Molar Masses. Gas Mixtures and Partial Pressures. The Behavior of Real Gases. Atmospheric Carbon Dioxide, the Greenhouse Effect, and Global Warming. 11. LIQUIDS, SOLIDS, AND MATERIALS. The Liquid State. Vapor Pressure. Phase Changes: Solids, Liquids, and Gases. Water: An Important Liquid with Unusual Properties. Types of Solids. Crystalline Solids. Network Solids. Metals, Semiconductors, and Insulators. 12. CHEMICAL 55

KINETICS: RATES OF REACTIONS. Reaction Rate. Effect of Concentration on Reaction Rate. Rate Law and Order of Reaction. A Nanoscale View: Elementary Reactions. Temperature and Reaction Rate: The Arrhenius Equation. Rate Laws for Elementary Reactions. Reaction Mechanisms. Catalysts and Reaction Rate. Enzymes: Biological Catalysts. Catalysts in Industry. 13. CHEMICAL EQUILIBRIUM. Characteristics of Chemical Equilibrium. The Equilibrium Constant. Determining Equilibrium Constants. The Meaning of the Equilibrium Constant. Using Equilibrium Constants. Shifting a Chemical Equilibrium: Le Chatelier s Principle. Equilibrium at the Nanoscale. Controlling Chemical Reactions: The Haber-Bosch Process. 14. THE CHEMISTRY OF SOLUTES AND SOLUTIONS. Solubility and Intermolecular Forces. Enthalpy, Entropy, and Dissolving Solutes. Solubility and Equilibrium. Temperature and Solubility. Pressure and Dissolving Gases in Liquids: Henry s Law. Solution Concentration: Keeping Track of Units. Vapor Pressures, Boiling Points, Freezing Points, and Osmotic Pressures of Solutions. 15. ACIDS AND BASES. The Brønsted- Lowry Concept of Acids and Bases. Carboxylic Acids and Amines. The Autoionization of Water. The ph Scale. Ionization Constants of Acids and Bases. Molecular Structure and Acid Strength. Problem Solving Using Ka and Kb. Acid-Base Reactions of Salts. Lewis Acids and Bases. 16. ADDITIONAL AQUEOUS EQUILIBRIA. Buffer Solutions. Acid-Base Titrations. Solubility Equilibria and the Solubility Product Constant, Ksp. Factors Affecting Solubility. Precipitation: Will It Occur? 17. THERMODYNAMICS: DIRECTIONALITY OF CHEMICAL REACTIONS. Reactant-Favored and Product- Favored Processes. Chemical Reactions and Dispersal of Energy. Measuring Dispersal of Energy: Entropy. Calculating Entropy Changes. Entropy and the Second Law of Thermodynamics. Gibbs Free Energy. Gibbs Free Energy Changes and Equilibrium Constants. Gibbs Free Energy and Maximum Work. Conservation of Gibbs Free Energy. Thermodynamic and Kinetic Stability. 18. ELECTROCHEMISTRY AND ITS APPLICATIONS. Redox Reactions. Using Half-Reactions to Understand Redox Reactions. Electrochemical Cells. Electrochemical Cells and Voltage. Using Standard Reduction Potentials. E and Gibbs Free Energy. Effect of Concentration on Cell Potential. Common Batteries. Fuel Cells. Electrolysis: Causing Reactant-Favored Reactions to Occur. Counting Electrons. Corrosion: Product-Favored Redox Reactions. 19. NUCLEAR CHEMISTRY. The Nature of Radioactivity. Nuclear Reactions. Stability of Atomic Nuclei. Rates of Disintegration Reactions. Nuclear Fission. Nuclear Fusion. Nuclear Radiation: Effects and Units. APPENDICES. Appendix A. Problem Solving and Mathematical Operations. General Problem-Solving Strategies. Numbers, Units, and Quantities. Precision, Accuracy, and Significant Figures. Electronic Calculators. Exponential or Scientific Notation. Logarithms. Quadratic Equations. Graphing. Appendix B. Units, Equivalences, and Conversion Factors. Units of the International System (SI). Conversion of Units for Physical Quantities. Appendix C. Physical Constants and Sources of Data. Appendix D. Ground-State Electron Configurations of Atoms. Appendix E. Naming Hydrocarbons. Hydrocarbons. Appendix F. Ionization Constants for Weak Acids at 25 C. Appendix G. Ionization Constants for Weak Bases at 25 C. Appendix H. Solubility Product Constants for Some Inorganic Compounds at 25 C. Appendix I. Standard Reduction Potentials in Aqueous Solution at 25 C. Appendix J. Selected Thermodynamic Values. Answers to Problem- Solving Practice Problems. Answers to Exercises. Answers to Selected Questions for Review and Thought. 2010, 848pp, Paperback, 9780495561293 PRINCIPLES OF MODERN CHEMISTRY, INTERNATIONAL EDITION, 7E David W. Oxtoby, Pomona College; H. Pat Gillis, University of California - Los Angeles; Alan Campion, University of Texas at Austin Long considered the standard for honors and high-level mainstream general chemistry courses, PRINCIPLES OF MODERN CHEMISTRY, 7e, International Edition continues to set the standard as the most modern, rigorous, and chemically and mathematically accurate text on the market. Thoroughly revised throughout 56

to strengthen its sound atoms first approach, this authoritative text now features new and updated content, and more mathematically accurate and artistic atomic and molecular orbital art. In addition, the text is now more student friendly without compromising its rigor. End-of-chapter study aids now focus on only the most important key objectives, equations and concepts, making it easier for students to locate chapter content, while new applications to a wide range of disciplines, such as biology, chemical engineering, biochemistry, and medicine deepen students understanding of the relevance of chemistry beyond the classroom. NEW TO THIS EDITION An UPDATED AND REVISED ATOMS FIRST APPROACH that enables the development of the subject from a unified and consistent molecular perspective. New features include: a rewritten Chapter 7 (Bonding in Organic Molecules), with new images that create a look-and-feel similar to that of Organic chemistry textbooks; and a completely revised suite of chapters (17-20) that introduces molecular electrochemistry at the freshman level for the first time, and treats kinetics, nuclear chemistry and molecular spectroscopy and photochemistry at the same level and depth, and from the same point of view, as the rest of the book. NEW CONNECTIONS TO SECTIONS emphasize applications of chemistry to a wide range of disciplines such as biology, chemical engineering, biochemistry, and medicine. NEW REAL-WORLD APPLICATIONS demonstrate how chemistry is used in the everyday world, in settings from business and industry to hospitals and laboratories. A DEEPER LOOK SECTIONS now appear at the end of each chapter to give students an in-depth look at the physical origins of observed chemical behavior without interrupting the flow of each chapter. RESTRUCTURED END-OF-CHAPTER STUDY AIDS, which now only include the most important key objectives, equations, and concepts, make it easier for students to locate content within the chapter NEW FULLY PARAMETERIZED END-OF-CHAPTER QUESTIONS IN OWL, written specifically for this text, encourage students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. AN ATOMS FIRST APPROACH places coverage of structure and bonding early in the text (Chapter 4-6), taking students right into the core topics of the course and helping them build a strong conceptual understanding of chemistry. A UNIQUE APPROACH TO LEARNING CHEMICAL PRINCIPLES emphasizes the scientific process from observation to application, placing general chemistry into perspective for serious-minded science and engineering students. MATHEMATICALLY ACCURATE MOLECULAR ORBITAL ART helps students visualize how orbital equations translate into the shapes of the orbitals. A FOCUS ON PROBLEM SOLVING. Problems are grouped into three categories: 1) Paired problems in the first set are grouped by section, with answers to the odd-numbered paired problems collected in Appendix G so students can check their answer to the first problem in a pair before undertaking the second parallel problem. 2) Additional Problems (unpaired) provide further applications of the principles developed in the chapter. 3) Cumulative Problems integrate material from the chapter with topics presented earlier in the book. More challenging problems are integrated throughout the problem sets and are indicated with asterisks. UNIT 1: INTRODUCTION TO THE STUDY OF MODERN CHEMISTRY. 1. The Atom in Modern Chemistry. 2. Chemical Formulas, Chemical Equations, and Reaction Yields. UNIT 2: CHEMICAL BONDING AND MOLECULAR STRUCTURE. 3. Chemical Bonding: The Classical Description. 4. Introduction to Quantum Mechanics. 5. Quantum Mechanics and Atomic Structure. 6. Quantum Mechanics and Molecular Structure. 7. Bonding in Organic Molecules. 8. Bonding in Transition Metal Compounds and Coordination Complexes. UNIT 3: KINETIC MOLECULAR DESCRIPTION OF THE STATES OF MATTER. 9. The Gaseous State. 10. Solids, Liquids, and Phase Transitions. 11. Solutions. UNIT 4: EQUILIBRIUM IN CHEMICAL REACTIONS. 12. Thermodynamic Processes and Thermochemistry. 13. Spontaneous Processes and Thermodynamic Equilibrium. 14. Chemical Equilibrium. 15. Acid Base 57

Equilibria. 16. Solubility and Precipitation Equilibria. 17. Electrochemistry. UNIT 5: RATES OF CHEMICAL AND PHYSICAL PROCESSES. 18. Chemical Kinetics. 19. Nuclear Chemistry. 20. Molecular Spectroscopy and Photochemistry. UNIT 6: MATERIALS. 21. Structure and Bonding in Solids. 22. Inorganic Materials. 23. Polymeric Materials and Soft Condensed Matter. 2012, 1280pp, Paperback, 9781111427832 STANDARD AND MICROSCALE EXPERIMENTS IN GENERAL CHEMISTRY, 5E Carl B. Bishop, Clemson University; Muriel B. Bishop, Clemson University; Kenneth W. Whitten, University of Georgia This comprehensive lab manual contains a wide array of experiments without sacrificing organizational clarity and includes categories on Energy, Kinetics, and Equilibrium. All experiments have undergone significant testing before being finalized, and many microscale experiments have been added to allow for more efficient and cost-effective means of conducting experiments. NEW TO THIS EDITION The Fifth Edition includes a helpful reference correlation guide that links each experiment to corresponding topics in selected Brooks/Cole general chemistry textbooks. Several additional labs will be available online for instructors at http://chemistry.brookscole.com. The Fifth Edition is accompanied by a comprehensive Laboratory Instructor s Manual, consisting of Important Reminders, Special Apparatus and Equipment, Chemicals, and Unknowns sections for each experiment. (available online at http://chemistry. brookscole.com.) Answers to Pre- and Post-Laboratory Assignments are available at the Brooks/Cole Chemistry Resource Center (http://chemistry.brookscole.com), as well as in a printed format available upon request STANDARD AND MICROSCALE EXPERIMENTS IN GENERAL CHEMISTRY is noted for its strong emphasis on safety procedures and precision, which leads to a successful laboratory experience for students. Pre-Laboratory Questions help students understand the chemical principles before beginning the experiments. The Background feature precedes groups of experiments to help students associate theory with experiments. Report Forms allow space for observations and interpretations. Post-Laboratory Questions are designed to be answered during the experiment and can be removed for grading. The large quantity of micro-scale experiments ensures that instructors have a wide-ranging selection and allow for more efficient and cost-effective means of conducting experiments. Part 1: EQUIPMENT. A. Common Laboratory Safety Equipment. B. Common Laboratory Glassware. C. Common Equipment. Part 2: LABORATORY TECHNIQUES. A. Handling Chemicals. Solids. Liquids. B. Determination of Mass and Weight. Triple-Beam and Platform Balances. Toploading Balances. C. Volumetric Techniques - The Measurements of Volume. Graduated Cylinders. Volumetric Pipets. Burets and Titration Procedures. Volumetric Flasks. D. Laboratory Gas Burner. E. Heating And Evaporating Liquids. F. Separation Techniques. Gravity Filtration. Vacuum Filtration. Use of Centrifuges. G. Ignition of Crucible and Precipitates. H. Working and Handling Glass. Cutting Glass. Fire Polishing Glass. Bending Glass. Inserting Glass Tubing, Thermometers, and Funnel Stems into Corks and Rubber Stoppers. I. Collecting Gases. Testing for Odor. Collection for Gases. An Improvised Fume Hood. J. Spectrophotometer. Calibration and Use of Spectrophotometer. Measurements of Sample. K. Treatment of Experimental Data. Significant Figures. Report Average Values. L. ph Meter. M. Melting And 58

Boiling Determination. Melting Point Determination. Boiling Point Determination. An Exercise in Chemical Safety and Laboratory Rules. Part 3: EXPERIMENTS (* MICRO EXPERIMENTS). 1.* Background: Review of Simple Mathematics (Experiment 1*). Experiment 2. Density of Solids and Liquids: Mass/Volume Measurements. Experiment 3. Indirect Gravimetric Determination of a Hydrated Compound in a Mixture. Experiment 4. Percent Copper and Formula Weight of a Copper Compound 65. 2. Background: Solutions, Solubility and Separation Techniques. Experiment 5.* Solubilities. Experiment 6. Separation of the Components of a Mixture. Experiment 7. Chromatography. 3. Background: Chemical Reactions in Aqueous Solutions and Syntheses. Experiment 8.* Hydrogen Ions, ph, and Indicators. Experiment 9.* Identify Eight Metal Ions by Reactions with Anions. Experiment 10.*Identify Ten Inorganic Compounds by Their Inter-Chemical Reactions. Experiment 11.*The Formula of a Precipitated Compound. Experiment 12. A Sequence of Chemical Reactions. Experiment 13. Synthesis of a Compound (Alum) from Scrap Aluminum. 4. Background: Periodic Table and Periodicity. Experiment 14. Molecular Models: Lewis Dot Formulas, VSEPR Theory, and Valence Bond Theory. Experiment 15.* Chemical Periodicity of the Halide Ions. Experiment 16.* Relative Reactivity of Metals and the Activity Series. 5. Background: Mole, Molecular Weight and Gas Laws. Experiment 17. Indirect Determination of the Masses of Pieces of Magnesium. Experiment 18. Density of Gases. Experiment 19. The Molecular Weight of a Volatile Compound. Experiment 20. Standard Molar Volume of a Gas. 6. Colligative Properties. Experiment 21. The Molecular Weight of a Compound by Freezing Point Depression Measurement. 7. Backgrounds: Acids-Bases. Experiment 22.* Acid Base Titration Curves Using: I. An Indicator Color- Reference II. Micro-pH Meter (micro-scale). Experiment 23. Acid Base Titrations: Analysis of Acid Solutions of Unknown Concentrations (macro-scale). Experiment 24. Action of Antacid Tablets. 8. Background: Reduction- Oxidation Reactions. Experiment 25.* Voltaic and Electrolytic Cells. Experiment 26.* Reduction-Oxidation Titrations (both micro and macro). 9. Background: Energy. Experiment 27. Heat Energy Associated with Chemical and Physical Changes. Experiment 28. Heats of Neutralization and Hess Law. 10. Background: Kinetics. Experiment 29.* Factors that Influence the Rates of Reaction. Experiment 30.* Rates of Chemical Reactions. 11. Background: Equilibrium. Experiment 31.* Chemical Equilibrium--An Introduction. Experiment 32. Spectrophotometric Determination of an Equilibrium Constant. Experiment 33. The Spectrophotometric Determination of the Formula for a Complex Species. Experiment 34.*Solubility Products of Insoluble Salts. Experiment 35. Determination of Ka from Measurements of ph. 12. Background: Descriptive Chemistry. Experiment 36. Oxygen and Some Oxides. Experiment 37. Nitrogen and Its Compounds. Experiment 38.* The Anions of Sulfur. 13. Background: Introduction to Organic Chemistry. Experiment 39.* Organic Qualitative Analysis. Experiment 40. Commercial Esters--Aspirin and Oil of Wintergreen. Experiment 41. Polymers. Experiment 42. Preparation and Properties of Soaps: Properties of Detergents. Appendix A: Logarithms and ph. Appendix B: Formulas, Ionic Charges and Names for Some Common Ions. Appendix C: Classification of Acids. Appendix D: Classification of Bases. Appendix E: Solubility Rules for Common Inorganic Compounds. Appendix F: Vapor Pressure of Water Near Room Temperature. Appendix G: Molecular and Ionic Chemical Equations. Appendix H: Concentrations and Primary Standards. Appendix I: Units of Measurement. 2004, 592pp, Paperback, 9780534424572 STUDY GUIDE FOR EBBING/GAMMON S GENERAL CHEMISTRY, 10E Darrell D. Ebbing, Wayne State University; Steven D. Gammon, Western Washington University This useful resource reinforces skills with activities and practice problems for each chapter. After completing the end-of-chapter exercises, students will be able to check their answers for the odd-numbered questions. 2013, 300pp, Paperback, 9781111989408 59

practice applying the concepts of the core text. 2014, 400pp, Paperback, 9781133933540 STUDY GUIDE FOR MOORE/STANITSKI S CHEMISTRY: THE MOLECULAR SCIENCE, 5E Michael Sanger, Middle Tennessee State University Study more effectively and improve your performance at exam time with this guide! The Study Guide for CHEMISTRY: THE MOLECULAR SCIENCE, FOURTH EDITION contains helpful learning tools, such as brief notes on chapter sections with examples, review of key terms, and practice tests (with answers). 2015, 272pp, Paperback, 9781285778662 STUDY GUIDE FOR ZUMDAHL/ ZUMDAHL S CHEMISTRY, 9E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Susan A. Zumdahl, University of Illinois, Urbana-Champaign Study more effectively and improve your performance at exam time with this comprehensive guide. The study guide includes: chapter summaries that highlight the main themes, study goals with section references, solutions to all textbook Example problems, and over 1,500 practice problems for all sections of the textbook. The Study Guide helps you organize the material and practice applying the concepts of the core text. 2014, 496pp, Paperback, 9781133611509 STUDY GUIDE FOR WHITTEN/DAVIS/ PECK/STANLEY S CHEMISTRY, 10TH, 10E Kenneth W. Whitten, University of Georgia; Raymond E. Davis, University of Texas, Austin; Larry Peck, Texas A&M University; George G. Stanley, Louisiana State University Study more effectively and improve your performance at exam time with this comprehensive guide. The guide includes chapter summaries that highlight the main themes; study goals with section references; lists of important terms; a preliminary test for each chapter that provides an average of 80 drill and concept questions; and answers to the preliminary tests. The Study Guide helps you organize the material and SURVIVAL GUIDE FOR GENERAL CHEMISTRY WITH MATH REVIEW, 2E Charles H. Atwood, University of Georgia Available free when packaged with any Cengage textbook or available separately for a minimal cost at www.cengagebrain.com, this survival guide focuses on helping you practice for exams by showing you how 60

to solve difficult problems by dissecting them into manageable chunks. The guide includes three levels of proficiency questions A, B, and minimal to quickly build your confidence as you master the knowledge you need to succeed in the course. Module 1: Metric System, Dimensional Analysis, Significant Figures, and Density. Module 2: Understanding Chemical Formulas. Module 3: Chemical Nomenclature. Module 4: The Mole Concept. Module 5: Chemical Reaction Stoichiometry. Module 6: Types of Chemical Reactions. Module 7: Electronic Structure of Atoms. Module 8: Chemical Periodicity. Module 9: Chemical Bonding. Module 10: Molecular Shapes. Module 11: Hybridization and Polarity of Molecules. Module 12: Acids and Bases. Module 13: States of Matter. Module 14: Solutions. Module 15: Heat Transfer, Calorimetry, and Thermodynamics. Module 16: Chemical Kinetics. Module 17: Gas Phase Equilibria. Module 18: Aqueous Equilibria. Module 19: Electrochemistry. Module 20: Nuclear Chemistry. Math Review. 2008, 216pp, Paperback, 9780495387510 Inorganic Chemistry DESCRIPTIVE INORGANIC, COORDINATION, AND SOLID STATE CHEMISTRY, INTERNATIONAL EDITION, 3E Glen E. Rodgers, Allegheny College This proven, sophomore-level text introduces the basics of coordination, solid-state, and descriptive main-group chemistry in a uniquely accessible manner, featuring a less is more approach. This approach allows you to present concepts and applications that you find particularly important and fascinating. Consistent with the less is more philosophy, the book does not review topics covered in introductory courses, but rather moves directly into topics central to inorganic chemistry. Written in a conversational prose style that is enjoyable and easy to understand, this book presents not only the basic theories and methods of inorganic chemistry (in three self-standing sections), but also a great deal of the history and applications of the discipline. The new edition features new art, more diversified applications, and a new icon system. And to better help students understand how the seemingly disparate topics of the periodical table connect, the book offers revised coverage of the author s Network of Interconnected Ideas on new full color endpapers, as well as on a convenient tear-out card. The author s presentation does not assume prerequisites of organic or physical chemistry. NEW TO THIS EDITION INCREASED EMPHASIS ON THE NETWORK OF INTERCONNECTED IDEAS. To better help students understand how the seemingly disparate topics of the periodical table connect, the book offers revised coverage of the author s Network of Interconnected Ideas including a new icon system, full color endpapers, and a convenient tear-out card. REVISED VISUALS. The text s art program has been revised for more clarity, and a new icon system makes the Network of Interconnected Ideas art better connect. UPDATED APPLICATIONS. The applications in Chapter 6 have been updated and diversified, and now cover more transition metals. In addition, the applications in the survey of periodic table groups chapters (12-19) have been updated. REORDERED APPENDIXES. The book s appendix have been reorganized to make them easier to use. SELF-CONTAINED SECTIONS. Coordination, solid state, and descriptive inorganic chemistry are presented in self-contained sections. The reader can begin in any one of these sections without becoming frustrated at references to material already learned. These self-standing chapters also allow instructors the flexibility to present material in any order. 61

A FOCUS ON UNDERSTANDING THE PERIODIC TABLE. The author systematically builds a network of interconnected ideas to develop reader confidence and to forge an understanding of the periodic table. THOUGHT QUESTIONS. These questions, embedded within the body of the text, encourage students to construct and organize ideas, thought patterns, and concepts, and to go beyond merely memorizing groups of facts or trends. Students must think their way through the material. A FOCUS ON PROBLEM SOLVING. Approximately 1,000 problems challenge students to apply what they have learned to new situations and aid in building a deeper understanding of the material. In addition, a significant number of problems require short explanatory paragraphs, emphasizing the importance of writing in the discipline of chemistry. A HISTORICAL PERSPECTIVE. A historical perspective is integrated throughout the text to give students an increased appreciation of the centuries of human endeavor that have led to our present understanding of the chemical world around us. A WIDE RANGE OF APPLICATIONS show students the practical uses of inorganic chemistry through the discussion of such diverse subjects as heavy metal poisoning and antidotes, nuclear fusion, battery technology, fluoridation, radon as a carcinogen, and automobile air bags. 1. The Evolving Realm of Inorganic Chemistry. PART 1: COORDINATION CHEMISTRY. 2. An Introduction to Coordination Chemistry. 3. Structures of Coordination Compounds. 4. Bonding Theories for Coordination Compounds. 5. Rates and Mechanisms of Reactions of Coordination Compounds. 6. Applications of Coordination Compounds. PART 2: SOLID-STATE CHEMISTRY. 7. Solid-State Structures. 8. Solid-State Energetics. PART 3: DESCRIPTIVE CHEMISTRY OF THE REPRESENTATIVE ELEMENTS. 9. Building a Network of Ideas to Make Sense of the Periodic Table. 10. Hydrogen and Hydrides. 11. Oxygen, Aqueous Solutions, and the Acid-Base Character of Oxides and Hydroxides. 12. Group 1A: The Alkali Metals. 13. Group 2A: The Alkaline- Earth Metals. 14. The Group 3A Elements. 15. The Group 4A Elements. 16. Group 5A: The Pnicogens. 17. Sulfur, Selenium, Tellurium, and Polonium. 18. Group 7A: The Halogens. 19. Group 8A: The Noble Gases. Introductory / Preparatory Chemistry A BEGINNER S GUIDE TO SCIENTIFIC METHOD, INTERNATIONAL EDITION, 4E Stephen S. Carey, Portland Community College This concise yet comprehensive guide provides an introduction to the scientific method of inquiry as well as detailed coverage of the many misapplications of scientific method that define pseudoscience. Compact enough to be used as a supplementary book in a science class, yet thorough enough in its coverage to be used as a core text in a class on scientific method, this text assists students in using the scientific method to design and assess experiments. NEW TO THIS EDITION The explanations have been thoroughly to ensure clarity and readability for the student audience. The discussion of causation in Chapter 3 has been greatly expanded. In Chapter 4, the basic framework for discussing experimental design has been revised to center on false confirmation and rejection. In Chapter 5, the discussion of probability and statistical inference is greatly simplified. Each section now begins with and explains all points in terms of recent causal studies. Two new pseudoscientific fallacies have been added and the text now contains many new and recent illustrations of all the fallacies. Dozens of new exercises and examples have been added to every chapter. End of chapter concept quizzes have been added. 2012, 656pp, Paperback, 9781111427153 62

An introduction to the scientific method which acknowledges that good science must remain utterly open to revision. Over one hundred practical, relevant exercises and examples address common conceptual issues and pitfalls confronted in students own practices of scientific learning. Real-life examples from scientific literature provide immediate practical applications of the concepts encountered in the book. Preface. 1. SCIENCE. Just What is Science? Asking Why. Scientific Method. The Consequences of Science. Scientific Method in Daily Life. Things to Come. Exercises 2. OBSERVATION. Making Accurate Observations. Anomalous Phenomena. Observing Anomalies. The Burden of Proof. Concept Quiz. Exercises 3. EXPLANATION. Explanation, Theory and Hypothesis. Causation. Correlation. Causal Mechanisms. Underlying Processes. Laws. Function. The Interdependence of Explanatory Methods. Rival Explanations and Ockham s Razor. Explanation and Description. Ultimate Explanations. Concept Quiz. Exercises. 4. EXPERIMENTATION. The Basic Method. Confirmation and Rejection. Designing a Good Test. Real World Experiments. How Not to Design a Test. Conceptual Vagueness. Testing Extraordinary Claims. Predictive Clarity. Bias and Expectation. Concept Quiz. Exercises. 5. ESTABLISHING CAUSAL LINKS. Causal Studies. Ruling Out Chance. Multiple Causal Factors. Randomized, Prospective and Retrospective Studies. Reading Between the Lines. Concept Quiz. Exercises. 6. FALLACIES IN THE NAME OF SCIENCE. What is a Fallacy? False Anomalies. Questionable Arguments by Elimination. Illicit Causal Inferences. Unsupported Analogies and Similarities. Untestable Explanations and Predictions. Empty Jargon. Ad Hoc Rescues. Exploiting Uncertainty. Science and Pseudoscience. Concept Quiz. Exercises. FURTHER READING INDEX 2012, 160pp, Paperback, 9781111726010 BASIC CHEMISTRY, 7E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Seventh Edition of Zumdahl and DeCoste s bestselling INTRODUCTORY CHEMISTRY: A FOUNDATION that combines enhanced problem-solving structure with substantial pedagogy to enable students to become strong independent problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the solution. This step-by-step approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to real-life experiences in chapter-opening discussions and Chemistry in Focus boxes.the Seventh Edition now adds a questioning pedagogy to in-text examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant number of revised end-ofchapter questions. The book s unsurpassed teaching and learning resources include a robust technology package that now offers a choice between OWL: Online Web Learning and Enhanced WebAssign. NEW TO THIS EDITION A significantly improved full color art program makes chemistry easier to understand for visual learners. The text s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what 63

questions the students should be asking as they solve problems. A new section in Chapter 8 explains why it is so important to become a good problem-solver. The authors have revised a significant number of the end-of-chapter questions (approximately 20%). The Seventh Edition is now supported by both OWL: Online Web Learning, the number one online learning system for chemistry, and Enhanced WebAssign. Both are available with e-books. Exercises and models such as worked-out examples, self-check exercises, and skill development boxes support the authors step-by-step problem-solving method. End-of-chapter material includes key terms, a summary of important facts, questions and problems arranged in matched pairs and keyed to chapter sections, additional problems that incorporate material from multiple sections, in-class discussion questions, and Cumulative Reviews that test concepts from preceding chapters. The text builds and refreshes fundamental math skills such as scientific notation, rounding, and rearranging equations. In addition, Math Tips, indicated by icons throughout, help students as they perform calculations. The book is also available in alternative versions: INTRODUCTORY CHEMISTRY; A FOUNDATION, which includes five additional chapters that cover equilibrium, oxidation-reduction reactions and electrochemistry, radioactivity and nuclear energy, organic chemistry, and biochemistry.(chapters 1-21) and INTRODUCTORY CHEMISTRY, which include additional coverage of equilibrium, oxidationreduction reactions, electrochemistry, radioactivity, and nuclear energy (Chapters 1-19). 1. CHEMISTRY: AN INTRODUCTION. Chemistry: An Introduction. Chemistry in Focus: Dr. Ruth Cotton Hero. What Is Chemistry? Solving Problems Using a Scientific Approach. Chemistry in Focus: A Mystifying Problem. The Scientific Method. Learning Chemistry. Chemistry in Focus: Chemistry: An Important Component of Your Education. 2. MEASUREMENTS AND CALCULATIONS. Scientific Notation. Units. Chemistry in Focus: Critical Units! Measurements of Length, Volume, and Mass. Chemistry in Focus: Measurement: Past, Present, and Future. Uncertainty in Measurement. Significant Figures. Problem Solving and Dimensional Analysis. Temperature Conversions: An Approach to Problem Solving. Chemistry in Focus: Tiny Thermometers. Density. 3. MATTER. Matter. Physical and Chemical Properties and Changes. Elements and Compounds. Mixtures and Pure Substances. Chemistry in Focus: Concrete An Ancient Material Made New. Separation of Mixtures. Cumulative Review for Chapters 1-3. 4. CHEMICAL FOUNDATIONS: ELEMENTS, ATOMS, AND IONS. The Elements. Chemistry in Focus: Trace Elements: Small but Crucial. Symbols for the Elements. Dalton s Atomic Theory. Chemistry in Focus: No Laughing Matter. Formulas of Compounds. The Structure of the Atom. Chemistry in Focus: Glowing Tubes for Signs, Television Sets, and Computers. Introduction to the Modern Concept of Atomic Structure. Isotopes. Chemistry in Focus: Isotope Tales. Introduction to the Periodic Table. Chemistry in Focus: Putting the Brakes on Arsenic. Natural States of the Elements. Ions Compounds That Contain Ions. 5. NOMENCLATURE. Naming Compounds. Chemistry in Focus: Sugar of Lead. Naming Binary Compounds That Contain a Metal and a Nonmetal (Types I and II). Naming Binary Compounds That Contain Only Nonmetals (Type III). Naming Binary Compounds: A Review. Naming Compounds That Contain Polyatomic Ions. Naming Acids. Writing Formulas from Names. Cumulative Review for Chapters 4-5. 6. CHEMICAL REACTIONS: AN INTRODUCTION. Evidence for a Chemical Reaction. Chemical Equations. Balancing Chemical Equations. Chemistry in Focus: The Beetle That Shoots Straight. 7. REACTIONS IN AQUEOUS SOLUTIONS. Predicting Whether a Reaction Will Occur. Reactions in Which a Solid Forms. Describing Reactions in Aqueous Solutions. Reactions That Form Water: Acids and Bases. Reactions of Metals with Nonmetals (Oxidation-Reduction). Ways to Classify Reactions. Chemistry in Focus: Do We Age by Oxidation? Chemistry in Focus: Oxidation- Reduction Reactions Launch the Space Shuttle. Other Ways to Classify Reactions. Cumulative Review for Chapters 6-7. 8. CHEMICAL COMPOSITION. Counting by Weighing. Chemistry in Focus: Plastic That Talks and Listens! Atomic Masses: Counting Atoms by Weighing. The Mole. Molar Mass. Percent Composition 64

of Compounds. Formulas of Compounds. Calculation of Empirical Formulas. Calculation of Molecular Formulas. 9. CHEMICAL QUANTITIES. Information Given by Chemical Equations. Mole Mole Relationships. Mass Calculations Chemistry in Focus: Methyl Alcohol: Fuel with a Future? Calculations Involving a Limiting Reactant. Percent Yield. Cumulative Review for Chapters 8-9. 10. ENERGY. The Nature of Energy. Temperature and Heat. Exothermic and Endothermic Processes. Thermodynamics. Measuring Energy Changes. Chemistry in Focus: Coffee: Hot and Quick(lime). Chemistry in Focus: Nature Has Hot Plants. Chemistry in Focus: Firewalking: Magic or Science? Thermochemistry (Enthalpy). Chemistry in Focus: Methane: An Important Energy Source. Hess s Law. Quality Versus Quantity of Energy. Energy and Our World. Chemistry in Focus: Veggie Gasoline? Energy as a Driving Force. 11. MODERN ATOMIC THEORY. Rutherford s Atom. Electromagnetic Radiation. Chemistry in Focus: Light as a Sex Attractant. Chemistry in Focus: Atmospheric Effects 307. Emission of Energy by Atoms. The Energy Levels of Hydrogen. The Bohr Model of the Atom. The Wave Mechanical Model of the Atom. The Hydrogen Orbitals. The Wave Mechanical Model: Further Development. Electron Arrangements in the First Eighteen Atoms on the Periodic Table. Chemistry in Focus: A Magnetic Moment. Electron Configurations and the Periodic Table. Chemistry in Focus: The Chemistry of Bohrium. Atomic Properties and the Periodic Table. Chemistry in Focus: Fireworks. 12. CHEMICAL BONDING. Types of Chemical Bonds. Electronegativity. Bond Polarity and Dipole Moments. Stable Electron Configurations and Charges on Ions. Chemistry in Focus: Composite Cars. Ionic Bonding and Structures of Ionic Compounds. Lewis Structures. Lewis Structures of Molecules with Multiple Bonds. Chemistry in Focus: Hiding Carbon Dioxide. Chemistry in Focus: Broccoli Miracle Food? Molecular Structure. Molecular Structure: The VSEPR Model. Chemistry in Focus: Taste It s the Structure That Counts. Molecular Structure: Molecules with Double Bonds. Chemistry in Focus: Minimotor Molecule. Cumulative Review for Chapters 10-12. 13. GASES. Pressure. Pressure and Volume: Boyle s Law. Volume and Temperature: Charles s Law. Volume and Moles: Avogadro s Law. The Ideal Gas Law. Chemistry in Focus: Snacks Need Chemistry, Too! Dalton s Law of Partial Pressures. Laws and Models: A Review. The Kinetic Molecular Theory of Gases. The Implications of the Kinetic Molecular Theory. Gas Stoichiometry. 14. LIQUIDS AND SOLIDS. Water and Its Phase Changes. Energy Requirements for the Changes of State. Chemistry in Focus: Whales Need Changes of State. Intermolecular Forces. Evaporation and Vapor Pressure. The Solid State: Types of Solids. Bonding in Solids. Chemistry in Focus: Metal with a Memory. 15. SOLUTIONS. Solubility. Chemistry in Focus: Green Chemistry. Solution Composition: An Introduction. Solution Composition: Mass Percent. Solution Composition: Molarity. Dilution. Stoichiometry of Solution Reactions. Neutralization Reactions. Solution Composition: Normality. Cumulative Review for Chapters 13-15. 16. ACIDS AND BASES. Acids and Bases. Chemistry in Focus: Gum That Foams. Acid Strength. Chemistry in Focus: Carbonation A Cool Trick. Chemistry in Focus: Plants Fight Back. Water as an Acid and a Base. The ph Scale. Chemistry in Focus: Airplane Rash. Chemistry in Focus: Garden-Variety Acid-Base Indicators. Calculating the ph of Strong Acid Solutions. Buffered Solutions. APPENDIX. Using Your Calculator. Basic Algebra. Scientific (Exponential) Notation. Graphing Functions. SI Units and Conversion Factors. Solutions to Self-Check Exercises. Answers to Even-Numbered End-of-Chapter Questions and Exercises. Answers to Even-Numbered Cumulative Review. Exercises. Index/Glossary. Photo Credits. 2011, 640pp, Paperback, 9780538736374 BASIC CHEMISTRY, 8E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Eighth Edition of Zumdahl and DeCoste s bestselling BASIC CHEMISTRY, 8e combines enhanced problem-solving structure with substantial pedagogy to enable students to become strong independent 65

problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the solution. This step-by-step approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to reallife experiences in chapter-opening discussions and Chemistry in Focus boxes (with many new ones added). Almost all of the in-text examples are now Interactive Examples and available online. These computer-based examples throughout the text require students to think through the Example step-by-step rather than simply scan the written Example in the text as many students do. New Critical Thinking boxes have been added. Many images have been significantly updated according to a new art style program to better serve visual learners. The Chapter Review section has been reorganized with a new structure along with a major revision to the review content. Key Terms have been updated throughout. A significant number of end-of-chapter questions have been added and revised. A new end-of-chapter question section titled ChemWork has been added and students can work on these types of problems online. NEW TO THIS EDITION In Chapter 9, the treatment of stoichiometry has been enhanced by the addition of a new section on limiting reactants, which emphasizes calculating the amounts of products that can be obtained from each reactant. Students are taught how to select a limiting reactant both by comparing the amounts of reactants present and by calculating the amounts of products that can be formed by complete consumption of each reactant. Interactive Examples, new for this edition, were added to engage students in the problem solving process as they are reading the text. These Interactive Examples require student input for each step in the example. The computer asks questions in the same way a teacher would when explaining a new concept. Critical Thinking questions have been added throughout the text to emphasize the importance of conceptual learning. These are particularly useful for generating class discussion. New ChemWork end-of chapter problems have been added throughout the text. These problems test students understanding of core concepts from each chapter. Students who need help can get assistance through a series of online hints. The hints are usually in the form of interactive questions that guide students through the problem-solving process. Students cannot receive the correct answer from the computer; rather, it encourages students to continue working through the hints to arrive at the answer. ChemWork problems in the text can be worked using the online system or as pencil-and-paper problems. Many of the Chemistry in Focus boxes have been revised and new ones added with up-to-date topics such as Gorilla glass, nanocars, and using breath analysis to diagnose disease. The #1 online homework and learning system for chemistry, OWLv2, is available for this text--now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader, a new ebook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new ipad-compatible ChemWork activities, visualizations, tutorials, and simulations. The book s full color art program has been modified and updated as needed to better serve visual learners. In addition, the art has been reconfigured for better clarity, glassware illustrations have been updated, and the orbital art has been redesigned all according to a new art and style program. Many new photos have been updated to give the textbook more relevance 66

while also providing a contemporary look. The text s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. Almost all of the in-text examples are now Interactive Examples and available online. These computerbased examples throughout the text require students to think through the Example step-by-step rather than simply scan the written Example in the text as many students do. 1. Chemistry: An Introduction. 2. Measurements and Calculations. 3. Matter. 4. Chemical Foundations: Elements, Atoms, and Ions. 5. Nomenclature. 6. Chemical Reactions: An Introduction. 7. Reactions in Aqueous Solutions. 8. Chemical Composition. 9. Chemical Quantities. 10. Energy. 11. Modern Atomic Theory. 12. Chemical Bonding. 13. Gases. 14. Liquids and Solids. 15. Solutions. 16. Acids and Bases. 2015, 608pp, Paperback, 9781285453149 CHEMISTRY FOR SPM Poh Bee Lee ; Loh Yew Lee ; Looi Chui Yean; N.Sivaneson Concept maps. Learning objectives. SPM Specimen Paper. Practice exercises. Detailed answers for self-assessment. CHAPTER 1 : Introduction to Chemistry CHAPTER 2: The Structure of the Atom CHAPTER 3: Chemical Formulae and Equations CHAPTER 4 : The Periodic Table of Elements CHAPTER 5 : Chemical Bonds CHAPTER 6 : Electrochemistry CHAPTER 7 : Acids and Bases CHAPTER 8 : Salts CHAPTER 9 : Manufactured Substances in Industry (FORM 5 ) CHAPTER 1: Rate of Reaction CHAPTER 2 : Carbon Compounds CHAPTER 3 : Oxidation and Reduction CHAPTER 4 : Thermochemistry CHAPTER 5 : Chemicals for Consumers SPM Specimen Chemistry Paper Answers Appendix 2011, 640pp, Paperback, 9789671014400, ESSENTIAL ALGEBRA FOR CHEMISTRY STUDENTS, 2E David W. Ball, Cleveland State University Available free when packaged with any Cengage textbook or available separately for a minimal cost at www.cengagebrain.com, this short book is designed to help you build confidence and competency in the essential mathematics skills necessary to survive in general chemistry. Each chapter focuses on a specific type of skill and has worked-out examples to show how these skills translate to chemical problem solving. NEW TO THIS EDITION REFERENCES TO OWL: This edition includes references to OWL material, which is being incorporated into all of Brooks/Cole s GOB and general chemistry texts. These online algebra skills exercises serve as additional practice of some of the skills in the book. EXTENSIVELY EDITED AND REVISED: We have edited and revised this text to underscore the basic skills students need for algebra in chemistry. Numerous examples and exercises, with answers, as well as problems specifically designed for use with 67

calculators. This book is adaptable because it is not text-specific; however, the ordering of chapters mimics the order of how much of the material is covered in introductory courses. The initial chapters serve as a useful baseline algebra review for all beginning chemistry students, with later chapters covering skills that are more specific to particular types of quantitative chemical problem solving. Preface. 1. Numbers, Units, and Scientific Notation. 2. Arithmetic Evaluation. 3. Significant Figures. 4. Converting Units. 5. Using Chemical Reactions to Make Conversion Factors. 6. Using Mathematical Formulas. 7. Advanced Math Topics. 8. Making Graphs. Index. 2006, 192pp, Paperback, 9780495013273 INTRODUCTION TO BASIC CHEMISTRY, INTERNATIONAL EDITION, 7E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Seventh Edition of INTRODUCTION TO BASIC CHEMISTRY, 7e, International Edition includes the first 16 chapters of INTRODUCTION TO CHEMISTRY: A FOUNDATION, 7e, International Edition. This new edition features a more explicit problem-solving pedagogy to help students develop critical thinking tools they can use in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and concluding by encouraging students to test their own understanding of the solution. This step-by-step approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to reallife experiences in chapter-opening discussions and Chemistry in Focus boxes. The Seventh Edition now adds a questioning pedagogy to in-text examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant number of revised end-ofchapter questions. The book s unsurpassed teaching and learning resources include a robust technology package that is now supported by OWL: Online Web Learning. NEW TO THIS EDITION A significantly improved full color art program makes chemistry easier to understand for visual learners. The text s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. A new section in Chapter 8 explains why it is so important to become a good problem-solver. The Seventh Edition is now supported by both OWL: Online Web Learning, the number one online learning system for chemistry. Exercises and models such as worked-out examples, self-check exercises, and skill development boxes support the authors step-by-step problem-solving method. End-of-chapter material includes key terms, a summary of important facts, questions and problems arranged in matched pairs and keyed to chapter sections, additional problems that incorporate material from multiple sections, in-class discussion questions, and Cumulative Reviews that test concepts from preceding chapters. The text builds and refreshes fundamental math skills such as scientific notation, rounding, and rearranging equations. In addition, Math Tips, indicated by icons throughout, help students as they perform calculations. 68

The book is also available in alternative versions: INTRODUCTION TO CHEMISTRY; A FOUNDATION, International Edition, which includes five additional chapters that cover equilibrium, oxidation-reduction reactions and electrochemistry, radioactivity and nuclear energy, organic chemistry, and biochemistry. (Chapters 1-21) and INTRODUCTION TO CHEMISTRY, International Edition which include additional coverage of equilibrium, oxidation-reduction reactions, electrochemistry, radioactivity, and nuclear energy (Chapters 1-19). 1. CHEMISTRY: AN INTRODUCTION. Chemistry: An Introduction. Chemistry in Focus: Dr. Ruth Cotton Hero. What Is Chemistry? Solving Problems Using a Scientific Approach. Chemistry in Focus: A Mystifying Problem. The Scientific Method. Learning Chemistry. Chemistry in Focus: Chemistry: An Important Component of Your Education. 2. MEASUREMENTS AND CALCULATIONS. Scientific Notation. Units. Chemistry in Focus: Critical Units! Measurements of Length, Volume, and Mass. Chemistry in Focus: Measurement: Past, Present, and Future. Uncertainty in Measurement. Significant Figures. Problem Solving and Dimensional Analysis. Temperature Conversions: An Approach to Problem Solving. Chemistry in Focus: Tiny Thermometers. Density. 3. MATTER. Matter. Physical and Chemical Properties and Changes. Elements and Compounds. Mixtures and Pure Substances. Chemistry in Focus: Concrete An Ancient Material Made New. Separation of Mixtures. Cumulative Review for Chapters 1-3. 4. CHEMICAL FOUNDATIONS: ELEMENTS, ATOMS, AND IONS. The Elements. Chemistry in Focus: Trace Elements: Small but Crucial. Symbols for the Elements. Dalton s Atomic Theory. Chemistry in Focus: No Laughing Matter. Formulas of Compounds. The Structure of the Atom. Chemistry in Focus: Glowing Tubes for Signs, Television Sets, and Computers. Introduction to the Modern Concept of Atomic Structure. Isotopes. Chemistry in Focus: Isotope Tales. Introduction to the Periodic Table. Chemistry in Focus: Putting the Brakes on Arsenic. Natural States of the Elements. Ions Compounds That Contain Ions. 5. NOMENCLATURE. Naming Compounds. Chemistry in Focus: Sugar of Lead. Naming Binary Compounds That Contain a Metal and a Nonmetal (Types I and II). Naming Binary Compounds That Contain Only Nonmetals (Type III). Naming Binary Compounds: A Review. Naming Compounds That Contain Polyatomic Ions. Naming Acids. Writing Formulas from Names. Cumulative Review for Chapters 4-5. 6. CHEMICAL REACTIONS: AN INTRODUCTION. Evidence for a Chemical Reaction. Chemical Equations. Balancing Chemical Equations. Chemistry in Focus: The Beetle That Shoots Straight. 7. REACTIONS IN AQUEOUS SOLUTIONS. Predicting Whether a Reaction Will Occur. Reactions in Which a Solid Forms. Describing Reactions in Aqueous Solutions. Reactions That Form Water: Acids and Bases. Reactions of Metals with Nonmetals (Oxidation-Reduction). Ways to Classify Reactions. Chemistry in Focus: Do We Age by Oxidation? Chemistry in Focus: Oxidation- Reduction Reactions Launch the Space Shuttle. Other Ways to Classify Reactions. Cumulative Review for Chapters 6-7. 8. CHEMICAL COMPOSITION. Counting by Weighing. Chemistry in Focus: Plastic That Talks and Listens! Atomic Masses: Counting Atoms by Weighing. The Mole. Molar Mass. Percent Composition of Compounds. Formulas of Compounds. Calculation of Empirical Formulas. Calculation of Molecular Formulas. 9. CHEMICAL QUANTITIES. Information Given by Chemical Equations. Mole Mole Relationships. Mass Calculations Chemistry in Focus: Methyl Alcohol: Fuel with a Future? Calculations Involving a Limiting Reactant. Percent Yield. Cumulative Review for Chapters 8-9. 10. ENERGY. The Nature of Energy. Temperature and Heat. Exothermic and Endothermic Processes. Thermodynamics. Measuring Energy Changes. Chemistry in Focus: Coffee: Hot and Quick(lime). Chemistry in Focus: Nature Has Hot Plants. Chemistry in Focus: Firewalking: Magic or Science? Thermochemistry (Enthalpy). Chemistry in Focus: Methane: An Important Energy Source. Hess s Law. Quality Versus Quantity of Energy. Energy and Our World. Chemistry in Focus: Veggie Gasoline? Energy as a Driving Force. 11. MODERN ATOMIC THEORY. Rutherford s Atom. Electromagnetic Radiation. Chemistry in Focus: Light as a Sex Attractant. Chemistry in Focus: Atmospheric Effects 307. Emission of Energy by Atoms. The Energy Levels of Hydrogen. The Bohr Model of the Atom. The Wave Mechanical Model of the Atom. The Hydrogen Orbitals. The Wave Mechanical Model: Further Development. Electron Arrangements in the First Eighteen Atoms on the Periodic Table. Chemistry in Focus: A Magnetic Moment. Electron Configurations and the Periodic Table. Chemistry in Focus: The Chemistry of Bohrium. Atomic Properties 69

and the Periodic Table. Chemistry in Focus: Fireworks. 12. CHEMICAL BONDING. Types of Chemical Bonds. Electronegativity. Bond Polarity and Dipole Moments. Stable Electron Configurations and Charges on Ions. Chemistry in Focus: Composite Cars. Ionic Bonding and Structures of Ionic Compounds. Lewis Structures. Lewis Structures of Molecules with Multiple Bonds. Chemistry in Focus: Hiding Carbon Dioxide. Chemistry in Focus: Broccoli Miracle Food? Molecular Structure. Molecular Structure: The VSEPR Model. Chemistry in Focus: Taste It s the Structure That Counts. Molecular Structure: Molecules with Double Bonds. Chemistry in Focus: Minimotor Molecule. Cumulative Review for Chapters 10-12. 13. GASES. Pressure. Pressure and Volume: Boyle s Law. Volume and Temperature: Charles s Law. Volume and Moles: Avogadro s Law. The Ideal Gas Law. Chemistry in Focus: Snacks Need Chemistry, Too! Dalton s Law of Partial Pressures. Laws and Models: A Review. The Kinetic Molecular Theory of Gases. The Implications of the Kinetic Molecular Theory. Gas Stoichiometry. 14. LIQUIDS AND SOLIDS. Water and Its Phase Changes. Energy Requirements for the Changes of State. Chemistry in Focus: Whales Need Changes of State. Intermolecular Forces. Evaporation and Vapor Pressure. The Solid State: Types of Solids. Bonding in Solids. Chemistry in Focus: Metal with a Memory. 15. SOLUTIONS. Solubility. Chemistry in Focus: Green Chemistry. Solution Composition: An Introduction. Solution Composition: Mass Percent. Solution Composition: Molarity. Dilution. Stoichiometry of Solution Reactions. Neutralization Reactions. Solution Composition: Normality. Cumulative Review for Chapters 13-15. 16. ACIDS AND BASES. Acids and Bases. Chemistry in Focus: Gum That Foams. Acid Strength. Chemistry in Focus: Carbonation A Cool Trick. Chemistry in Focus: Plants Fight Back. Water as an Acid and a Base. The ph Scale. Chemistry in Focus: Airplane Rash. Chemistry in Focus: Garden-Variety Acid-Base Indicators. Calculating the ph of Strong Acid Solutions. Buffered Solutions. APPENDIX. Using Your Calculator. Basic Algebra. Scientific (Exponential) Notation. Graphing Functions. SI Units and Conversion Factors. Solutions to Self-Check Exercises. Answers to Even-Numbered End-of-Chapter Questions and Exercises. Answers to Even-Numbered Cumulative Review. Exercises. Index/Glossary. Photo Credits. 2011, 688pp, Paperback, 9780538736640 INTRODUCTION TO CHEMICAL PRINCIPLES, 7E A Laboratory Approach, International Edition Susan A. Weiner, West Valley College ; Blaine Harrison The seventh edition of this superb lab manual offers 36 class-tested experiments, suitable for introductory, preparatory, and health science chemistry courses and texts, including INTRODUCTORY CHEMISTRY: AN ACTIVE LEARNING APPROACH, 4e, INTERNATIONAL EDITION by Cracolice and Peters. Experiments in this lab manual teach students to collect and analyze experimental data and provide them with a strong foundation for further course work in general chemistry. This edition offers instructors a wide variety of experiments to customize their laboratory program, including many microscale experiments. All experiments can be completed in a three-hour laboratory period. As in the Sixth Edition, there are Work Pages for each experiment as well as Report Sheets for students to take notes and record experimental data and results, which facilitate instructor grading of experiments. NEW TO THIS EDITION The new edition features 11 worksheets covering the major topics of introductory chemistry. The worksheets can be used to enhance the lab experience or as supplementary homework. Complete solutions are available in the Instructor s Manual. The Seventh Edition also features four new experiments: Experiment 27: Organic Nomenclature, Experiment 30: Esters, Experiment 34: Lipids, and Experiment 36: Enzymes. Several experiments have also been revised to provide clearer direction and more detail in the Procedure section. 70

Duplicate Work Pages and Report Sheets for each experiment offer a convenient and efficient way for students to record their data as they work and yield clean, easy-to-grade reports. Advance Study Assignments, to be completed before performing the experiments, require students to read the experiment before executing the lab, thus enabling them to complete the experiment in a safe and timely fashion. Sample Calculations are presented to acquaint the student with the type of calculations they will be required to perform for the experiment. The lab manual features a variety of experiments for inorganic and organic chemistry so that it may accompany many different chemistry textbooks from introductory inorganic chemistry to allied health chemistry. SAFETY IN THE LABORATORY. LABORATORY PROCEDURES. EXPERIMENTS: 1. Properties and Changes of Matter (m). 2. The Chemistry of Some Household Products. 3. Separation of Cations by Paper Chromatography (m). 4. Densities of Liquids and Solids. 5. Simplest Formula of a Compound (m). 6. Hydrates (m). 7. Percentage of Oxygen in Potassium Chlorate. 8. Calorimetry. 9. Chemical Names and Formulas: A Study Assignment. 10. Chemical Equations: A Study Assignment. 11. Mole Ratio for a Chemical Reaction (m). 12. Types of Chemical Reactions (m). 13. Qualitative Analysis of Some Common Ions (m). 14. Separation of Cations. 15. Molecular Models: A Study Assignment. 16. Molar Volume of a Gas (m). 17. Molar Mass Determination by Freezing-Point Depression. 18. The Conductivity of Solutions: A Demonstration. 19. Net Ionic Equations: A Study Assignment. 20. Titration of Acids and Bases I. 21. Titration of Acids and Bases II. 22. Determination of a Chemical Equation. 23. A Study of Reaction Rates. 24. Chemical Equilibrium (m). 25. Measurement of ph with Indicators. 26. Introduction to Oxidation-Reduction Reactions (m). 27. Organic Nomenclature. 28. Hydrocarbons and Alcohols. 29. Aldehydes, Ketones, and Carboxylic Acids. 30. Esters. 31. Preparation of Aspirin. 32. Preparation and Properties of a Soap. 33. Carbohydrates. 34. Lipids. 35. Amino Acids and Proteins. 36. Enzymes. WORKSHEETS: 1. Significant Figures. 2. Dimensional Analysis. 3. Avogrado s Number- Moles. 4. Formula Writing. 5. Equation Balancing-Types of Reactions. 6. Stoichiometry. 7. Atomic Structure. 8. Gases. 9. Solutions. 10. Oxidation-Reduction. 11. Acids and Bases. Appendix. 2010, 480pp, Paperback, 9781439046647 INTRODUCTION TO CHEMISTRY, 7E A Foundation, International Edition Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Seventh Edition of Zumdahl and DeCoste s best-selling INTRODUCTION TO CHEMISTRY: A FOUNDATION, International Edition that combines enhanced problem-solving structure with substantial pedagogy to enable students to become strong independent problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the solution. This step-by-step approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to real-life experiences in chapter-opening discussions and Chemistry in Focus boxes. The Seventh Edition now adds a questioning pedagogy to in-text examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant number of revised end-ofchapter questions. The book s unsurpassed teaching and learning resources include a robust technology 71

package that now offers OWL: Online Web Learning. NEW TO THIS EDITION The book s full color art program has been redrawn and reworked to make figures easier to follow and more aesthetically pleasing. In addition, labeling within the art has been reconfigured for better clarity, glassware illustrations have been updated, and the orbital art has been redesigned. The text s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. A new section in Chapter 8 explains why it is so important to become a good problem-solver. The Seventh Edition is now supported by both OWL: Online Web Learning, the number one online learning system for chemistry, and Enhanced WebAssign. Both are available with e-books. Exercises and models such as worked-out examples, self-check exercises, and skill development boxes support the authors step-by-step problem-solving method. End-of-chapter material includes key terms, a summary of important facts, questions and problems arranged in matched pairs and keyed to chapter sections, additional problems that incorporate material from multiple sections, in-class discussion questions, and Cumulative Reviews that test concepts from preceding chapters. The text builds and refreshes fundamental math skills such as scientific notation, rounding, and rearranging equations. In addition, Math Tips, indicated by icons throughout, help students as they perform calculations. The book is also available in alternative versions: INTRODUCTION TO BASIC CHEMISTRY, International Edition, which covers chemical concepts and applications through acids and bases (Chapters 1-16) and INTRODUCTION TO CHEMISTRY, International Edition, which also covers equilibrium, oxidationreduction reactions, electrochemistry, radioactivity, and nuclear energy (Chapters 1-19). 1. CHEMISTRY: AN INTRODUCTION. Chemistry: An Introduction. Chemistry in Focus: Dr. Ruth Cotton Hero. What Is Chemistry? Solving Problems Using a Scientific Approach. Chemistry in Focus: A Mystifying Problem. The Scientific Method. Learning Chemistry. Chemistry in Focus: Chemistry: An Important Component of Your Education. 2. MEASUREMENTS AND CALCULATIONS. Scientific Notation. Units. Chemistry in Focus: Critical Units! Measurements of Length, Volume, and Mass. Chemistry in Focus: Measurement: Past, Present, and Future. Uncertainty in Measurement. Significant Figures. Problem Solving and Dimensional Analysis. Temperature Conversions: An Approach to Problem Solving. Chemistry in Focus: Tiny Thermometers. Density. 3. MATTER. Matter. Physical and Chemical Properties and Changes. Elements and Compounds. Mixtures and Pure Substances. Chemistry in Focus: Concrete An Ancient Material Made New. Separation of Mixtures. Cumulative Review for Chapters 1-3. 4. CHEMICAL FOUNDATIONS: ELEMENTS, ATOMS, AND IONS. The Elements. Chemistry in Focus: Trace Elements: Small but Crucial. Symbols for the Elements. Dalton s Atomic Theory. Chemistry in Focus: No Laughing Matter. Formulas of Compounds. The Structure of the Atom. Chemistry in Focus: Glowing Tubes for Signs, Television Sets, and Computers. Introduction to the Modern Concept of Atomic Structure. Isotopes. Chemistry in Focus: Isotope Tales. Introduction to the Periodic Table. Chemistry in Focus: Putting the Brakes on Arsenic. Natural States of the Elements. Ions Compounds That Contain Ions. 5. NOMENCLATURE. Naming Compounds. Chemistry in Focus: Sugar of Lead. Naming Binary Compounds That Contain a Metal and a Nonmetal (Types I and II). Naming Binary Compounds That Contain Only Nonmetals (Type III). Naming Binary Compounds: A Review. Naming Compounds That Contain Polyatomic Ions. Naming Acids. Writing Formulas from Names. Cumulative Review for Chapters 4-5. 6. CHEMICAL REACTIONS: AN INTRODUCTION. Evidence for a Chemical Reaction. Chemical Equations. Balancing Chemical Equations. Chemistry in Focus: The Beetle That Shoots Straight. 7. REACTIONS IN AQUEOUS SOLUTIONS. Predicting Whether a Reaction Will Occur. Reactions in Which a Solid Forms. Describing Reactions in Aqueous Solutions. Reactions That Form Water: Acids and Bases. Reactions of Metals with Nonmetals (Oxidation-Reduction). Ways to Classify Reactions. Chemistry in Focus: Do We Age 72

by Oxidation? Chemistry in Focus: Oxidation-Reduction Reactions Launch the Space Shuttle. Other Ways to Classify Reactions. Cumulative Review for Chapters 6-7. 8. CHEMICAL COMPOSITION. Counting by Weighing. Chemistry in Focus: Plastic That Talks and Listens! Atomic Masses: Counting Atoms by Weighing. The Mole. Molar Mass. Percent Composition of Compounds. Formulas of Compounds. Calculation of Empirical Formulas. Calculation of Molecular Formulas. 9. CHEMICAL QUANTITIES. Information Given by Chemical Equations. Mole Mole Relationships. Mass Calculations Chemistry in Focus: Methyl Alcohol: Fuel with a Future? Calculations Involving a Limiting Reactant. Percent Yield. Cumulative Review for Chapters 8-9. 10. ENERGY. The Nature of Energy. Temperature and Heat. Exothermic and Endothermic Processes. Thermodynamics. Measuring Energy Changes. Chemistry in Focus: Coffee: Hot and Quick(lime). Chemistry in Focus: Nature Has Hot Plants. Chemistry in Focus: Firewalking: Magic or Science? Thermochemistry (Enthalpy). Chemistry in Focus: Methane: An Important Energy Source. Hess s Law. Quality Versus Quantity of Energy. Energy and Our World. Chemistry in Focus: Veggie Gasoline? Energy as a Driving Force. 11. MODERN ATOMIC THEORY. Rutherford s Atom. Electromagnetic Radiation. Chemistry in Focus: Light as a Sex Attractant. Chemistry in Focus: Atmospheric Effects 307. Emission of Energy by Atoms. The Energy Levels of Hydrogen. The Bohr Model of the Atom. The Wave Mechanical Model of the Atom. The Hydrogen Orbitals. The Wave Mechanical Model: Further Development. Electron Arrangements in the First Eighteen Atoms on the Periodic Table. Chemistry in Focus: A Magnetic Moment. Electron Configurations and the Periodic Table. Chemistry in Focus: The Chemistry of Bohrium. Atomic Properties and the Periodic Table. Chemistry in Focus: Fireworks. 12. CHEMICAL BONDING. Types of Chemical Bonds. Electronegativity. Bond Polarity and Dipole Moments. Stable Electron Configurations and Charges on Ions. Chemistry in Focus: Composite Cars. Ionic Bonding and Structures of Ionic Compounds. Lewis Structures. Lewis Structures of Molecules with Multiple Bonds. Chemistry in Focus: Hiding Carbon Dioxide. Chemistry in Focus: Broccoli Miracle Food? Molecular Structure. Molecular Structure: The VSEPR Model. Chemistry in Focus: Taste It s the Structure That Counts. Molecular Structure: Molecules with Double Bonds. Chemistry in Focus: Minimotor Molecule. Cumulative Review for Chapters 10-12. 13. GASES. Pressure. Pressure and Volume: Boyle s Law. Volume and Temperature: Charles s Law. Volume and Moles: Avogadro s Law. The Ideal Gas Law. Chemistry in Focus: Snacks Need Chemistry, Too! Dalton s Law of Partial Pressures. Laws and Models: A Review. The Kinetic Molecular Theory of Gases. The Implications of the Kinetic Molecular Theory. Gas Stoichiometry. 14. LIQUIDS AND SOLIDS. Water and Its Phase Changes. Energy Requirements for the Changes of State. Chemistry in Focus: Whales Need Changes of State. Intermolecular Forces. Evaporation and Vapor Pressure. The Solid State: Types of Solids. Bonding in Solids. Chemistry in Focus: Metal with a Memory. 15. SOLUTIONS. Solubility. Chemistry in Focus: Green Chemistry. Solution Composition: An Introduction. Solution Composition: Mass Percent. Solution Composition: Molarity. Dilution. Stoichiometry of Solution Reactions. Neutralization Reactions. Solution Composition: Normality. Cumulative Review for Chapters 13-15. 16. ACIDS AND BASES. Acids and Bases. Chemistry in Focus: Gum That Foams. Acid Strength. Chemistry in Focus: Carbonation A Cool Trick. Chemistry in Focus: Plants Fight Back. Water as an Acid and a Base. The ph Scale. Chemistry in Focus: Airplane Rash. Chemistry in Focus: Garden-Variety Acid-Base Indicators. Calculating the ph of Strong Acid Solutions. Buffered Solutions. 17. EQUILIBRIUM. How Chemical Reactions Occur. Conditions That Affect Reaction Rates. Chemistry in Focus: Protecting the Ozone. The Equilibrium Condition. Chemical Equilibrium: A Dynamic Condition. The Equilibrium Constant: An Introduction. Heterogeneous Equilibria. Le Châtelier s Principle. Applications Involving the Equilibrium Constant. Solubility Equilibria. Cumulative Review for Chapters 16-17. 18. OXIDATION-REDUCTION REACTIONS AND ELECTROCHEMISTRY. Oxidation-Reduction Reactions. Oxidation States. Oxidation-Reduction Reactions Between Nonmetals. Balancing Oxidation-Reduction Reactions by the Half-Reaction Method. Electrochemistry: An Introduction. Batteries. Corrosion. Chemistry in Focus: Stainless Steel: It s the Pits. Electrolysis. Chemistry in Focus: Water-Powered Fireplace. 19. RADIOACTIVITY AND NUCLEAR ENERGY. Radioactive Decay. Nuclear Transformations. Detection of Radioactivity and the Concept of Half-life. Dating by 73

Radioactivity. Chemistry in Focus: Dating Diamonds. Medical Applications of Radioactivity. Nuclear Energy. Nuclear Fission. Nuclear Reactors. Chemistry in Focus: Future Nuclear Power. Nuclear Fusion. Effects of Radiation. Chemistry in Focus: Nuclear Waste Disposal. 20. ORGANIC CHEMISTRY. Carbon Bonding. Alkanes. Structural Formulas and Isomerism. Naming Alkanes. Petroleum. Reactions of Alkanes. Alkenes and Alkynes. Aromatic Hydrocarbons. Naming Aromatic Compounds. Chemistry in Focus: Termite Mothballing. Functional Groups. Alcohols. Properties and Uses of Alcohols. Aldehydes and Ketones. Naming Aldehydes and Ketones. Carboxylic Acids and Esters. Polymers. Chemistry in Focus: The Chemistry of Music. Chemistry in Focus: Polymers Are Tacky. B21. BIOCHEMISTRY. Proteins. Primary Structure of Proteins. Secondary Structure of Proteins. Tertiary Structure of Proteins. Functions of Proteins. Enzymes. Chemistry in Focus: Urine Farming. Carbohydrates. Chemistry in Focus: Great Expectations? The Chemistry of Placebos. Nucleic Acids. Lipids. APPENDIX. Using Your Calculator. Basic Algebra. Scientific (Exponential) Notation. Graphing Functions. SI Units and Conversion Factors. Solutions to Self-Check Exercises. Answers to Even-Numbered End-of-Chapter Questions and Exercises. Answers to Even-Numbered Cumulative Review. Exercises. Index/ Glossary. Photo Credits. 2011, 848pp, Paperback, 9780538735438 INTRODUCTORY CHEMISTRY, 7E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Seventh Edition of Zumdahl and DeCoste s bestselling INTRODUCTORY CHEMISTRY: A FOUNDATION that combines enhanced problem-solving structure with substantial pedagogy to enable students to become strong independent problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the solution. This step-by-step approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to real-life experiences in chapter-opening discussions and Chemistry in Focus boxes.the Seventh Edition now adds a questioning pedagogy to in-text examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant number of revised end-ofchapter questions. The book s unsurpassed teaching and learning resources include a robust technology package that now offers a choice between OWL: Online Web Learning and Enhanced WebAssign. NEW TO THIS EDITION The book s full color art program has been redrawn and reworked to make figures easier to follow and more aesthetically pleasing. In addition, labeling within the art has been reconfigured for better clarity, glassware illustrations have been updated, and the orbital art has been redesigned. The text s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. A new section in Chapter 8 explains why it is so important to become a good problem-solver. The authors have revised a significant number of the end-of-chapter questions (approximately 20%). The Seventh Edition is now supported by both OWL: Online Web Learning, the number one online learning system for chemistry, and Enhanced WebAssign. Both are available with e-books. Exercises and models such as worked-out examples, self-check exercises, and skill development boxes 74

support the authors step-by-step problem-solving method. End-of-chapter material includes key terms, a summary of important facts, questions and problems arranged in matched pairs and keyed to chapter sections, additional problems that incorporate material from multiple sections, in-class discussion questions, and Cumulative Reviews that test concepts from preceding chapters. The text builds and refreshes fundamental math skills such as scientific notation, rounding, and rearranging equations. In addition, Math Tips, indicated by icons throughout, help students as they perform calculations. The book is also available in alternative versions: BASIC CHEMISTRY, which covers chemical concepts and applications through acids and bases (Chapters 1-16) and INTRODUCTORY CHEMISTRY, which also covers equilibrium, oxidation-reduction reactions, electrochemistry, radioactivity, and nuclear energy (Chapters 1-19). 1. CHEMISTRY: AN INTRODUCTION. Chemistry: An Introduction. Chemistry in Focus: Dr. Ruth Cotton Hero. What Is Chemistry? Solving Problems Using a Scientific Approach. Chemistry in Focus: A Mystifying Problem. The Scientific Method. Learning Chemistry. Chemistry in Focus: Chemistry: An Important Component of Your Education. 2. MEASUREMENTS AND CALCULATIONS. Scientific Notation. Units. Chemistry in Focus: Critical Units! Measurements of Length, Volume, and Mass. Chemistry in Focus: Measurement: Past, Present, and Future. Uncertainty in Measurement. Significant Figures. Problem Solving and Dimensional Analysis. Temperature Conversions: An Approach to Problem Solving. Chemistry in Focus: Tiny Thermometers. Density. 3. MATTER. Matter. Physical and Chemical Properties and Changes. Elements and Compounds. Mixtures and Pure Substances. Chemistry in Focus: Concrete An Ancient Material Made New. Separation of Mixtures. Cumulative Review for Chapters 1-3. 4. CHEMICAL FOUNDATIONS: ELEMENTS, ATOMS, AND IONS. The Elements. Chemistry in Focus: Trace Elements: Small but Crucial. Symbols for the Elements. Dalton s Atomic Theory. Chemistry in Focus: No Laughing Matter. Formulas of Compounds. The Structure of the Atom. Chemistry in Focus: Glowing Tubes for Signs, Television Sets, and Computers. Introduction to the Modern Concept of Atomic Structure. Isotopes. Chemistry in Focus: Isotope Tales. Introduction to the Periodic Table. Chemistry in Focus: Putting the Brakes on Arsenic. Natural States of the Elements. Ions Compounds That Contain Ions. 5. NOMENCLATURE. Naming Compounds. Chemistry in Focus: Sugar of Lead. Naming Binary Compounds That Contain a Metal and a Nonmetal (Types I and II). Naming Binary Compounds That Contain Only Nonmetals (Type III). Naming Binary Compounds: A Review. Naming Compounds That Contain Polyatomic Ions. Naming Acids. Writing Formulas from Names. Cumulative Review for Chapters 4-5. 6. CHEMICAL REACTIONS: AN INTRODUCTION. Evidence for a Chemical Reaction. Chemical Equations. Balancing Chemical Equations. Chemistry in Focus: The Beetle That Shoots Straight. 7. REACTIONS IN AQUEOUS SOLUTIONS. Predicting Whether a Reaction Will Occur. Reactions in Which a Solid Forms. Describing Reactions in Aqueous Solutions. Reactions That Form Water: Acids and Bases. Reactions of Metals with Nonmetals (Oxidation-Reduction). Ways to Classify Reactions. Chemistry in Focus: Do We Age by Oxidation? Chemistry in Focus: Oxidation-Reduction Reactions Launch the Space Shuttle. Other Ways to Classify Reactions. Cumulative Review for Chapters 6-7. 8. CHEMICAL COMPOSITION. Counting by Weighing. Chemistry in Focus: Plastic That Talks and Listens! Atomic Masses: Counting Atoms by Weighing. The Mole. Molar Mass. Percent Composition of Compounds. Formulas of Compounds. Calculation of Empirical Formulas. Calculation of Molecular Formulas. 9. CHEMICAL QUANTITIES. Information Given by Chemical Equations. Mole Mole Relationships. Mass Calculations Chemistry in Focus: Methyl Alcohol: Fuel with a Future? Calculations Involving a Limiting Reactant. Percent Yield. Cumulative Review for Chapters 8-9. 10. ENERGY. The Nature of Energy. Temperature and Heat. Exothermic and Endothermic Processes. Thermodynamics. Measuring Energy Changes. Chemistry in Focus: Coffee: Hot and Quick(lime). Chemistry in Focus: Nature Has Hot Plants. Chemistry in Focus: Firewalking: Magic or Science? Thermochemistry (Enthalpy). Chemistry in Focus: Methane: An Important Energy Source. Hess s Law. Quality Versus Quantity of Energy. Energy and Our World. Chemistry in Focus: Veggie Gasoline? Energy as a Driving Force. 11. MODERN 75

ATOMIC THEORY. Rutherford s Atom. Electromagnetic Radiation. Chemistry in Focus: Light as a Sex Attractant. Chemistry in Focus: Atmospheric Effects 307. Emission of Energy by Atoms. The Energy Levels of Hydrogen. The Bohr Model of the Atom. The Wave Mechanical Model of the Atom. The Hydrogen Orbitals. The Wave Mechanical Model: Further Development. Electron Arrangements in the First Eighteen Atoms on the Periodic Table. Chemistry in Focus: A Magnetic Moment. Electron Configurations and the Periodic Table. Chemistry in Focus: The Chemistry of Bohrium. Atomic Properties and the Periodic Table. Chemistry in Focus: Fireworks. 12. CHEMICAL BONDING. Types of Chemical Bonds. Electronegativity. Bond Polarity and Dipole Moments. Stable Electron Configurations and Charges on Ions. Chemistry in Focus: Composite Cars. Ionic Bonding and Structures of Ionic Compounds. Lewis Structures. Lewis Structures of Molecules with Multiple Bonds. Chemistry in Focus: Hiding Carbon Dioxide. Chemistry in Focus: Broccoli Miracle Food? Molecular Structure. Molecular Structure: The VSEPR Model. Chemistry in Focus: Taste It s the Structure That Counts. Molecular Structure: Molecules with Double Bonds. Chemistry in Focus: Minimotor Molecule. Cumulative Review for Chapters 10-12. 13. GASES. Pressure. Pressure and Volume: Boyle s Law. Volume and Temperature: Charles s Law. Volume and Moles: Avogadro s Law. The Ideal Gas Law. Chemistry in Focus: Snacks Need Chemistry, Too! Dalton s Law of Partial Pressures. Laws and Models: A Review. The Kinetic Molecular Theory of Gases. The Implications of the Kinetic Molecular Theory. Gas Stoichiometry. 14. LIQUIDS AND SOLIDS. Water and Its Phase Changes. Energy Requirements for the Changes of State. Chemistry in Focus: Whales Need Changes of State. Intermolecular Forces. Evaporation and Vapor Pressure. The Solid State: Types of Solids. Bonding in Solids. Chemistry in Focus: Metal with a Memory. 15. SOLUTIONS. Solubility. Chemistry in Focus: Green Chemistry. Solution Composition: An Introduction. Solution Composition: Mass Percent. Solution Composition: Molarity. Dilution. Stoichiometry of Solution Reactions. Neutralization Reactions. Solution Composition: Normality. Cumulative Review for Chapters 13-15. 16. ACIDS AND BASES. Acids and Bases. Chemistry in Focus: Gum That Foams. Acid Strength. Chemistry in Focus: Carbonation A Cool Trick. Chemistry in Focus: Plants Fight Back. Water as an Acid and a Base. The ph Scale. Chemistry in Focus: Airplane Rash. Chemistry in Focus: Garden-Variety Acid-Base Indicators. Calculating the ph of Strong Acid Solutions. Buffered Solutions. 17. EQUILIBRIUM. How Chemical Reactions Occur. Conditions That Affect Reaction Rates. Chemistry in Focus: Protecting the Ozone. The Equilibrium Condition. Chemical Equilibrium: A Dynamic Condition. The Equilibrium Constant: An Introduction. Heterogeneous Equilibria. Le Châtelier s Principle. Applications Involving the Equilibrium Constant. Solubility Equilibria. Cumulative Review for Chapters 16-17. 18. OXIDATION-REDUCTION REACTIONS AND ELECTROCHEMISTRY. Oxidation-Reduction Reactions. Oxidation States. Oxidation-Reduction Reactions Between Nonmetals. Balancing Oxidation-Reduction Reactions by the Half-Reaction Method. Electrochemistry: An Introduction. Batteries. Corrosion. Chemistry in Focus: Stainless Steel: It s the Pits. Electrolysis. Chemistry in Focus: Water-Powered Fireplace. 19. RADIOACTIVITY AND NUCLEAR ENERGY. Radioactive Decay. Nuclear Transformations. Detection of Radioactivity and the Concept of Half-life. Dating by Radioactivity. Chemistry in Focus: Dating Diamonds. Medical Applications of Radioactivity. Nuclear Energy. Nuclear Fission. Nuclear Reactors. Chemistry in Focus: Future Nuclear Power. Nuclear Fusion. Effects of Radiation. Chemistry in Focus: Nuclear Waste Disposal. 20. ORGANIC CHEMISTRY. Carbon Bonding. Alkanes. Structural Formulas and Isomerism. Naming Alkanes. Petroleum. Reactions of Alkanes. Alkenes and Alkynes. Aromatic Hydrocarbons. Naming Aromatic Compounds. Chemistry in Focus: Termite Mothballing. Functional Groups. Alcohols. Properties and Uses of Alcohols. Aldehydes and Ketones. Naming Aldehydes and Ketones. Carboxylic Acids and Esters. Polymers. Chemistry in Focus: The Chemistry of Music. Chemistry in Focus: Polymers Are Tacky. B21. BIOCHEMISTRY. Proteins. Primary Structure of Proteins. Secondary Structure of Proteins. Tertiary Structure of Proteins. Functions of Proteins. Enzymes. Chemistry in Focus: Urine Farming. Carbohydrates. Chemistry in Focus: Great Expectations? The Chemistry of Placebos. Nucleic Acids. Lipids. APPENDIX. Using Your Calculator. Basic Algebra. Scientific (Exponential) Notation. Graphing Functions. SI Units and Conversion Factors. Solutions to Self-Check Exercises. Answers to Even-Numbered 76

End-of-Chapter Questions and Exercises. Answers to Even-Numbered Cumulative Review. Exercises. Index/ Glossary. Photo Credits. 2011, 736pp, Paperback, 9780538736398 INTRODUCTORY CHEMISTRY, 5E An Active Learning Approach, International Edition Mark S. Cracolice, University of Montana; Edward I. Peters Teach the course your way with INTRODUCTORY CHEMISTRY, 5E, International Edition. This text allows you to tailor the order of chapters to accommodate your particular needs, not only by presenting topics so they never assume prior knowledge but also by including any and all necessary preview or review information needed to learn that topic. The authors question-and-answer presentation allows students to actively learn chemistry while studying an assignment. This approach is reflected in three words of advice and encouragement that are repeated throughout the book: Learn It Now! This edition integrates new features such as outstanding technological resources, coached problems in a two-column format, and enhanced art and photography, all of which dovetail with the authors active learning approach. Even more flexibility is provided in the new edition by the Cengage YouBook, an electronic version of the text that features interactivity, integrated media, and additional algebra coverage. NEW TO THIS EDITION New Active Example Format: After observing students rush to apply an algorithm immediately after reading a problem statement, the authors redesigned the Active Example format. To encourage students to be less impulsive and slow down and analyze the problem statement before working on the solution, the first frame in every Active Example is labeled THINK BEFORE YOU WRITE. Subsequent steps are labeled as PLAN to help students consciously outline the solution to a problem. New Two-Column Design for Active Examples: As students actively work through and complete the Active Example solution in the right column, they can reveal the solution to each step in the left column, thereby receiving immediate feedback about their understanding of the concept as it is being formed. Each example is also now titled so that students can better identify the concept or problem-solving skill they are learning and can easily locate specific concepts to review when preparing for exams. New Practice Exercises and Solutions: To solidify the potentially fragile new knowledge that the student just constructed during the process of completing the Active Example, each Active Example is now immediately followed by a parallel Practice Exercise that covers the same concept as the companion Active Examples, but is typically slightly more challenging. By pairing the Active Examples with Practice Exercises, the book leads students toward improved conceptual understanding and problem-solving skills. Solutions to this edition s 241 Practice Exercises are provided in Appendix III. New End-of-Chapter Illustrations: More than 100 new photographs and line drawings have been added to the end-of-chapter Questions, Exercises, and Problems to better illustrate the macroscopic aspect of chemistry and allow students to see physical and chemical changes and common forms of industrial manufacturing processes, as well as better visualize the scenarios described in the questions. Enhanced Features in OWL. OWL now includes Student Self-Assessments, as well as the interactive customizable Cengage YouBook, a multimedia electronic version of the text. Portable Chapter-in-Review Cards: Designed to make anywhere, anytime studying easier, these detachable cards at the back of the book include chapter summaries of goals and key concepts and a chapter self-test with answers. Group Discussion Questions: These questions give students the opportunity to work together to develop their problem solving and conceptual understanding. 77

Flexible Format: The book has been structured so that any common sequence of topics is supported, allowing professors to present topics in any order they prefer. Thinking About Your Thinking Comments: Designed to encourage students to think the way chemists do and focus on critical thinking, these features help students develop broad thinking skills they can apply to new contexts in future chemistry courses, other academic disciplines, and throughout their lives. Section-Opening Learning Objectives: Identified as Goals, these objectives focus attention on what students are expected to learn or the skill they are expected to develop while studying the section. 1. Introduction to Chemistry; Introduction to Active Learning. 2. Matter and Energy. 3. Measurement and Chemical Calculations. 4. Introduction to Gases. 5. Atomic Theory: The Nuclear Model of the Atom. 6. Chemical Nomenclature. 7. Chemical Formula Relationships. 8. Chemical Reactions. 9. Chemical Change. 10. Quantity Relationships in Chemical Reactions. 11. Atomic Theory: The Quantum Model of the Atom. 12. Chemical Bonding. 13. Structure and Shape. 14. The Ideal Gas Law and Its Applications. 15. Gases, Liquids, and Solids. 16. Solutions. 17. Acid-Base (Proton-Transfer) Reactions. 18. Chemical Equilibrium. 19. Oxidation-Reduction (Redox) Reactions. 20. Nuclear Chemistry. 21. Organic Chemistry. 22. Biochemistry. Appendix I: Chemical Calculations. Appendix II: The SI System of Units. Glossary. Index. 2013, 848pp, Paperback, 9781133108115 INTRODUCTORY CHEMISTRY, 8E Steven S. Zumdahl, University of Illinois, Urbana-Champaign; Donald J. DeCoste, University of Illinois, Urbana-Champaign The Eighth Edition of Zumdahl and DeCoste s bestselling INTRODUCTORY CHEMISTRY that combines enhanced problem-solving structure with substantial pedagogy to enable students to become strong independent problem solvers in the introductory course and beyond. Capturing student interest through early coverage of chemical reactions, accessible explanations and visualizations, and an emphasis on everyday applications, the authors explain chemical concepts by starting with the basics, using symbols or diagrams, and conclude by encouraging students to test their own understanding of the solution. This step-by-step approach has already helped hundreds of thousands of students master chemical concepts and develop problem-solving skills. The book is known for its focus on conceptual learning and for the way it motivates students by connecting chemical principles to reallife experiences in chapter-opening discussions and Chemistry in Focus boxes. The Eighth Edition now adds a questioning pedagogy to in-text examples to help students learn what questions they should be asking themselves while solving problems, offers a revamped art program to better serve visual learners, and includes a significant number of revised end-ofchapter questions. NEW TO THIS EDITION The #1 online homework and learning system for chemistry, OWLv2, is available for this text--now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader, a new ebook with apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new ipadcompatible visualizations, tutorials, and simulations. 78

The book s full color art program has been modified and updated as needed to better serve visual learners. In addition, the art has been reconfigured for better clarity, glassware illustrations have been updated, and the orbital art has been redesigned all according to a new art and style program. Many new photos have been updated to give the textbook more relevance while also providing a contemporary look. The text s hallmark problem-solving pedagogy is enhanced by in-text examples that suggest what questions the students should be asking as they solve problems. Almost all of the in-text examples are now Interactive Examples and available online. These computerbased examples throughout the text require students to think through the Example step-by-step rather than simply scan the written Example in the text as many students do. New Critical Thinking boxes have been added at point-of-use throughout the text to emphasize the importance of conceptual learning. These are particularly useful for generating class discussion. In Section 8.4 Learning to Solve Problems is written specifically to help students better understand how to think their way through a problem. In Chapter 9, the treatment of stoichiometry has been enhanced by the addition of a new section on limiting reactants, which emphasizes calculating the amounts of products that can be obtained from each reactant. Students are taught how to select a limiting reactant both by comparing the amounts of reactants present and by calculating the amounts of products that can be formed by complete consumption of each reactant. The authors have revised a significant number of the end-of-chapter questions (over 10%) while adding a new section for ChemWork problems, which are also available online. The Eighth Edition is now supported by both OWL: Online Web Learning, the number one online learning system for chemistry, and Enhanced WebAssign. Both are available with e-books. Exercises and models such as worked-out examples, self-check exercises, and skill development boxes support the authors step-by-step problem-solving method. 1. Chemistry: An Introduction. 2. Measurements and Calculations. 3. Matter. 4. Chemical Foundations: Elements, Atoms, and Ions. 5. Nomenclature. 6. Chemical Reactions: An Introduction. 7. Reactions in Aqueous Solutions. 8. Chemical Composition. 9. Chemical Quantities. 10. Energy. 11. Modern Atomic Theory. 12. Chemical Bonding. 13. Gases. 14. Liquids and Solids. 15. Solutions. 16. Acids and Bases. 17. Equilibrium. 18. Oxidation Reduction Reactions and Electrochemistry. 19. Radioactivity and Nuclear Energy. 2015, 704pp, Paperback, 9781285453132 LAB MANUAL FOR ZUMDAHL/ DECOSTE S INTRODUCTORY CHEMISTRY: A FOUNDATION, 8TH, 8E John G. Little Includes 35 experiments and eight appendices that serve as useful references. 2015, 368pp, Paperback, 9781285845166 STUDY GUIDE FOR ZUMDAHL/ DECOSTE S INTRODUCTORY CHEMISTRY: A FOUNDATION, 8TH, 8E Donald J. DeCoste, University of Illinois, Urbana-Champaign The perfect way to prepare for exams, build problemsolving skills, and get the grade you want, this 79

Study Guide includes chapter discussions, key-term definitions, and practice chapter tests. 2015, 224pp, Paperback, 9781285845173 SURVIVAL GUIDE FOR INTRODUCTORY CHEMISTRY Charles H. Atwood, University of Georgia SURVIVAL GUIDE FOR GENERAL CHEMISTRY WITH MATH REVIEW, 2E Charles H. Atwood, University of Georgia Available free when packaged with any Cengage textbook, this survival guide focuses on helping students practice for exams by showing them how to solve difficult problems by dissecting them into manageable chunks. The guide includes three levels of proficiency questions A, B, and minimal to quickly build student confidence as they master the knowledge needed to succeed in the course. This book is also available for students to purchase separately at www. cengagebrain.com. Module 1: Metric System, Dimensional Analysis, Significant Figures, and Density. Module 2: Understanding Chemical Formulas. Module 3: Chemical Nomenclature. Module 4: The Mole Concept. Module 5: Chemical Reaction Stoichiometry. Module 6: Types of Chemical Reactions. Module 7: Electronic Structure of Atoms. Module 8: Chemical Periodicity. Module 9: Chemical Bonding. Module 10: Molecular Shapes. Module 11: Hybridization and Polarity of Molecules. Module 12: Acids and Bases. Module 13: States of Matter. Module 14: Solutions. Module 15: Heat Transfer, Calorimetry, and Thermodynamics. Module 16: Chemical Kinetics. Module 17: Gas Phase Equilibria. Module 18: Aqueous Equilibria. Module 19: Electrochemistry. Module 20: Nuclear Chemistry. Math Review. 2008, 216pp, Paperback, 9780495387510 Straightforward, thorough, packed with examples and exercises, and modeled after Atwood s widely popular CHEMISTRY SURVIVAL GUIDE, the new SURVIVAL GUIDE FOR INTRODUCTORY CHEMISTRY is everything your students need to survive and thrive in an introductory course. Designed as a reader s guide to an introductory textbook, the SURVIVAL GUIDE offers detailed step-by-step problem-solving sequences, giving students the competency and confidence they need to master the material and achieve optimal exam results. Coupled with a complementary math review, this brief but powerful resource covers the most fundamental aspects of introductory chemistry in a succinct series of essential modules. Student-friendly content: Key Terms, Concepts, and Equations highlight and clarify introductory chemistry issues for students, helping them to focus on essential information and to maximize their study time. Sample Exercises: Providing step-by-step instruction, Sample Exercises include detailed explanations that guide students in gaining a solid understanding of chemistry concepts and principles. Avoiding Pitfalls: Included throughout the text, Caution icons alert students to common mistakes and help them avoid such missteps, making chemistry more accessible and easier to understand. Tips and Tools: Problem Solving Tips give students additional insight for successfully working through exercises and strengthening their analytical skills. You can order the SURVIVAL GUIDE FOR INTRODUCTORY CHEMISTRY in a convenient, moneysaving package with either of these newer texts: 80

Zumdahl/Zumdahl, INTRODUCTORY CHEMISTRY, 6E or Craccolice/Peters, INTRODUCTORY CHEMISTRY: AN ACTIVE LEARNING APPROACH, 4E. Module 1. An Approach to Problem Solving. Module 2. Metric System, Significant Figures, Dimensional Analysis, and Density. Module 3. Matter and Energy. Module 4. Elements, Atoms and the Periodic Table. Module 5. Chemical Nomenclature. Module 6. Understanding Chemical Formulas and Using the Mole Concept. Module 7. Understanding Chemical Reaction Equations. Module 8. Chemical Reactions in Aqueous Solutions. Module 9. Chemical Reaction Stoichiometry. Module 10. Electronic Structure of Atoms. Module 11. Periodic Trends in Chemistry. Module 12. Chemical Bonding. Module 13. Molecular Shapes and Polarity. Module 14. Gases. Module 15. Liquids and Solids. Module 16. Solutions. Module 17. Acids and Bases. Module 18. Chemical Equilibrium. Module 19. Oxidation-Reduction Reactions and Electrochemistry. Module 20. Nuclear Chemistry. Math Review. 2009, 192pp, Paperback, 9780495828266 Liberal Arts Chemistry CHEM 2, 2E Chemistry in Your World (with OWLv2 24-Months Printed Access Card) John L. Hogg, Texas A&M University Created by the continuous feedback of a studenttested, faculty-approved process, CHEM2 delivers a visually appealing, succinct print component, tearout review cards for students and instructors, and a consistent online offering with CourseMate that includes an ebook in addition to a set of interactive digital tools -- all at a value-based price and proven to increase retention and outcomes. CHEM2 also offers Go Chemistry and Thinkwell mini-video lectures, as well as online homework available through the OWL learning system. NEW TO THIS EDITION END-OF-CHAPTER QUESTIONS have been added to nearly every chapter. POWERPOINT LECTURE SLIDES, completely customizable to your specific classroom needs, help you prep for class faster and more efficiently. NEW DETACHABLE EQUATION-SPECIFIC CARDS show students how to properly set up conversion and stoichiometric equations while they do their homework. Each card features a skeleton version of the equation as well as an example. A MORE USER-FRIENDLY, CHEMISTRY-SPECIFIC DESIGN reflects the needs of today s liberal arts students. The #1 online homework and learning system for chemistry, OWLv2, is available for this text--now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader, a new ebook withh apps and embedded video, audio, annotations, and activities. OWLv2 courses for Gen Chem, GOB, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text, 45 new visual exercises, and new ipad-compatible visualizations, tutorials, and simulations. EXTENSIVELY REORGANIZED CHAPTERS 2 AND 16 provide a better flow of subjects to enhance student understanding. THE UPDATED ART PROGRAM offers new and more relevant instructive images. DETACHABLE CHAPTER IN REVIEW CARDS, revised to match the text s narrative, give students a portable 81

study tool packed with pertinent information they can use to prepare for class. DETACHABLE INSTRUCTOR PREP CARDS -- now including a list of the major revisions in each chapter -- make class prep quick and easy and include a quick map of chapter content, a list of corresponding PowerPoint and video resources, additional examples, and suggested assignments and discussion questions. RELEVANT, REAL LIFE APPLICATIONS have been updated to reflect up-to-date issues affecting the chemical world. 1. Living in a World of Chemistry. 2. The Chemical View of Matter. 3. Atoms and the Periodic Table. 4. The Air We Breathe. 5. Chemical Bonding and States of Matter. 6. Carbon Dioxide and the Greenhouse Effect. 7. Chlorofl uorocarbons and the Ozone Layer. 8. Chemical Reactivity: Chemicals in Action. 9. Acid--Base Reactions. 10. Oxidation--Reduction Reactions. 11. Water, Water Everywhere but Not a Drop to Drink? 12. Energy and Hydrocarbons. 13. Nuclear Changes and Nuclear Power. 14. Organic Chemicals and Polymers. 15. The Chemistry of Life. 16. Nutrition: The Basis of Healthy Living. 17. Chemistry and Medicine. 18. The Chemistry of Useful Materials. 19. Feeding the World. Appendices (Answers to Try Its & Answers to Selected Problems). Index. 2015, 496pp, Paperback, 9781133962984 CHEM 4LTR (WITH REVIEW CARDS AND CHEMISTRY COURSEMATE WITH EBOOK PRINTED ACCESS CARD) Melvin Joesten, Vanderbilt University ; John L. Hogg, Texas A&M University; Donald R. Neu, Saint Cloud State University CHEM delivers exactly what today s students need --and want. Based on student and faculty feedback from nationwide interviews and focus groups, CHEM was developed through a student-tested, facultyapproved process. The result is a concise, engaging, and accessible textbook that presents the basic chemical principles faculty require within a framework of relevant, real world applications that liberal arts students can relate to. Delivered at a value price, CHEM accommodates the diverse lifestyles of today s learners, features a modern, open page design, and includes a wide array of print and online learning aids, including chapter-by-chapter study cards, self-quizzes, interactive flash cards, Go Chemistry and Thinkwell mini-video lectures, and online homework available through the OWL learning system. Shorter, comprehensive chapters in a modern design, along with a wealth of print and online teaching and learning aids, make this book ideal for today s students. Detachable Chapter in Review cards give students a portable study tool packed with pertinent information they can use to prepare for class. Detachable Instructor Prep cards make class prep quick and easy and include a quick map of chapter content, a list of corresponding PowerPoint and video resources, additional examples, and suggested assignments and discussion questions. Learning tools designed to meet a wide range of learning styles include interactive quizzes, animations, videos, interactive and printable flashcards, and additional essays. Relevant, real- life applications feature such topics as the nutritional basis of healthy living, medicines and drugs, pollution & the conservation of natural resources, and the agricultural production of food for an ever-expanding world population. 1. Living in a World of Chemistry. 2. The Chemical View of Matter. 3. Atoms and the Periodic Table. 4. The Air We Breathe and Some Major Atmospheric Pollutants. 5. Chemical Bonding and States of Matter. 6. Carbon Dioxide and the Greenhouse Effect. 7. Chlorofluorocarbons and the Ozone Layer. 8. Chemical Reactivity: Chemicals in Action. 9. Acid-Base Reactions. 10. Oxidation-Reduction Reactions. 11. Water, Water Everywhere, but Not a Drop to Drink? 12. Energy and 82

Hydrocarbons. 13. Nuclear Changes and Nuclear Power. 14. Organic Chemicals and Polymers. 15. The Chemistry of Life. 16. Nutrition: The Basis of Healthy Living. 17. Chemistry and Medicine. 18. The Chemistry of Useful Materials. 19. Feeding the World. 2011, 448pp, Paperback, 9780538738217 Organic Chemistry A MICROSCALE APPROACH TO ORGANIC LABORATORY TECHNIQUES, INTERNATIONAL EDITION, 5E Donald L. Pavia, Western Washington University; George S. Kriz, Western Washington University; Gary M. Lampman, Western Washington University; Randall G. Engel, North Seattle Community College From biofuels, green chemistry, and nanotechnology, this proven laboratory textbook provides the up-to-date coverage students need in their coursework and future careers. The book s experiments, all designed to utilize microscale glassware and equipment, cover traditional organic reactions and syntheses, the isolation of natural products, and molecular modeling and include project-based experiments and experiments that have a biological or health science focus. Updated throughout with new and revised experiments, new and revised essays, and revised and expanded techniques, the Fifth Edition is organized based on essays and topics of current interest. NEW TO THIS EDITION A new essay on Biofuels enhances this edition s in the news topics. Two new Green Chemistry experiments involve techniques such as solid phase extraction and the use of a microwave reaction system. In two experiments, chiral gas chromatography is now included in the analysis of the products obtained. Eight new experiments have been added: Experiment 2, Solubility; Experiment 27, Biodiesel; Experiment 34, Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes Using a Palladium Catalyst; Experiment 35, Grubbs-Catalyzed Metathesis of Eugenol with 1,4-Butanediol to Prepare a Natural Product; Experiment 48: Diels-Alder Reaction with Anthracene-9-methanol; Experiment 59, Synthesis of Naproxen (Aleve ) by Palladium Catalysis; Experiment 62, Green Epoxidation of Chalcones; and Experiment 63, Cyclopropanation of Chalcones. Four experiments have been revised: Experiment 31, An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol; Experiment 44, N,N-Diethylm-toluamide: The Insect Repellant OFF ; Experiment 52, Identification of Unknowns; and Experiment 56, Friedel-Crafts Acylation. Essays on Petroleum and Fossil Fuels and The Chemistry of Sweeteners have been revised. Four Techniques have been revised and expanded: Technique 7, Reaction Methods, has been extensively revised to include information on working under an inert atmosphere; Technique 12, Extractions, Separations, and Drying Agents, now includes new material on instructions on drawing separation schemes; Technique 25, Infrared Spectroscopy, now includes the use of ATR for infrared analysis of solids; and Technique 26, Nuclear Magnetic Resonance Spectroscopy, includes new material on analysis of diastereotopic protons. A new method of obtaining boiling points and monitoring distillations using a temperature probe with one of the Vernier devices or a digital thermometer has been introduced. The Cengage YouBook, an interactive, electronic version of the lab manual, allows students to print and bring to the lab bench only the parts of the book they need, as well as to watch videos showing how each technique is executed. Quizzes in the YouBook test whether students understand the technique, and results of the quiz can be submitted to the instructor prior to entering the lab. Open-ended experiments allow students to write 83

their own experimental procedures and make their own discoveries. PART I: INTRODUCTION TO BASIC LABORATORY TECHNIQUES. Experiment 1: Introduction to Microscale Laboratory. Experiment 2: Solubility. Experiment 3: Crystallization. Experiment 4: Extraction. Experiment 5: A Separation and Purification Scheme. Experiment 6: Chromatography. Experiment 7: Simple and Fractional Distillation. Experiment 8: Infrared Spectroscopy and Boiling Point Determination. ESSAY: Aspirin. Experiment 9: Acetylsalicylic Acid. ESSAY: Analgesics. Experiment 10: Isolation of the Active Ingredient in an Analgesic Drug. Experiment 11: Acetaminophen. ESSAY: Identification of Drugs. Experiment 12: TLC Analysis of Analgesic Drugs. ESSAY: Caffeine. Experiment 13: Isolation of Caffeine. ESSAY: Esters -- Flavors and Fragrances. Experiment 14: Isopentyl Acetate (Banana Oil). ESSAY: Terpenes and Phenylpropanoids. Experiment 15: Essential Oils: Extraction of Oil of Cloves by Steam Distillation. Essay: Stereochemical Theory of Odor. Experiment 16: Spearmint and Caraway Oil: (+)- and (-)- Carvones. Essay: The Chemistry of Vision. Experiment 17: Isolation of Chlorophyll and Carotenoid Pigments from Spinach. Essay: Ethanol and Fermentation Chemistry. Experiment 18 Ethanol from Sucrose. PART II: INTRODUCTION TO MOLECULAR MODELING. ESSAY: Molecular Modeling and Molecular Mechanics. Experiment 19: An Introduction to Molecular Modeling. ESSAY: Computational Chemistry -- Ab initio and Semiempirical Methods. Experiment 20: Computational Chemistry. PART III: PROPERTIES AND REACTIONS OF ORGANIC COMPOUNDS. Experiment 21: Reactivities of Some Alkyl Halides. Experiment 22: Nucleophilic Substitution Reactions: Competing Nucleophiles. Experiment 23: Synthesis of n-butyl Bromide and t-pentyl Chloride. Experiment 24: 4-Methylcyclohexene. ESSAY: Fats and Oils. Experiment 25: Methyl Stearate from Methyl Oleate. ESSAY: Petroleum and Fossil Fuels. Experiment 26: Gas Chromatographic Analysis of Gasolines. ESSAY: Biofuels. Experiment 27: Biodiesel. ESSAY: Green Chemistry. Experiment 28: Chiral Reduction of Ethyl Acetoacetate; Optical Purity Determination Using a Chiral Shift Reagent. Experiment 29: Nitration of Aromatic Compounds Using a Recyclable Catalyst. Experiment 30: Resolution of ( Phenylethylamine and Determination of Optical Purity. Experiment 31: An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol. Experiment 32: Multi-Step Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid. Experiment 33: Triphenylmethanol and Benzoic Acid. Experiment 34: Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes Using a Palladium Catalyst. Experiment 35: Grubbs-Catalyzed Metathesis of Eugenol with 1,4-Butanediol to Prepare a Natural Product. Experiment 36: Aqueous-based Organozinc Reactions. Experiment 37: The Aldol Condensation Reaction: Preparation of Benzalacetophenones (Chalcones). Experiment 38: Preparation of an Unsaturated Ketone via Michael and Aldol Condensation Reactions. Experiment 39: The Wittig Reaction: Preparation of 1,4-Diphenyl- 1,3-butadiene. Experiment 40: Relative Reactivities of Several Aromatic Compounds. Experiment 41: Nitration of Methyl Benzoate. ESSAY: Local Anesthetics. Experiment 42: Benzocaine. Experiment 43: Methyl Salicylate (Oil of Wintergreen). ESSAY: Pheromones: Insect Attractants and Repellents. Experiment 44: N,N-Diethyl-m-toluamide: The Insect Repellent OFF. ESSAY: Sulfa Drugs. Experiment 45: Sulfa Drugs: Preparation of Sulfanilamide. Essay: Polymers and Plastics. Experiment 46: Preparation and Properties of Polymers: Polyester, Nylon, and Polystyrene. Essay: Diels-Alder Reactions and Insecticides. Experiment 47: The Diels-Alder Reaction of Cyclopentadiene with Maleic Anhydride. Experiment 48: Diels-Alder Reaction with Anthracene-9-methanol. Experiment 49: Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. ESSAY:Fireflies and Photochemistry. Experiment 50: Luminol. ESSAY: The Chemistry of Sweeteners. Experiment 51: Analysis of a Diet Soft Drink by HPLC. PART IV: IDENTIFICATION OF ORGANIC SUBSTANCES. Experiment 52: Identification of Unknowns. PART V: PROJECT-BASED EXPERIMENTS. Experiment 53: Preparation of a C-4 or C-5 Acetate Ester. Experiment 54: Isolation of Essential Oils from Allspice, Cloves, Cumin, Caraway, Cinnamon, Fennel, or Star Anise. Experiment 55: Competing Nucleophiles in SN1 and SN2 Reactions: Investigations using 2-Pentanol and 3-Pentanol. Experiment 56: Friedel-Crafts Acylation. Experiment 57: The Analysis of Antihistamine Drugs by Gas Chromatography-Mass Spectrometry. Experiment 58: The Use of Organozinc Reagents in Synthesis: 84

An Exercise in Synthesis and Structure Proof by Spectroscopy. Experiment 59: Synthesis of Naproxen by Palladium Catalysis. Experiment 60: The Aldehyde Enigma. Experiment 61: Synthesis of Substituted Chalcones: A Guided-Inquiry Experience. Experiment 62: Green Epoxidation of Chalcones. Experiment 63: Cyclopropanation of Chalcones. Experiment 64: Michael and Aldol Condensation Reactions. Experiment 65: Esterification Reactions of Vanillin: The Use of NMR to Solve a Structure Proof Problem. Experiment 66: An Oxidation Puzzle. PART VI: THE TECHNIQUES. Technique 1: Laboratory Safety. Technique 2: The Laboratory Notebook, Calculations, and Laboratory Records. Technique 3: Laboratory Glassware: Care and Cleaning. Technique 4: How to Find Data for Compounds: Handbooks and Catalogues. Technique 5: Measurement of Volume and Weight. Technique 6: Heating and Cooling Methods. Technique 7: Reaction Methods. Technique 8: Filtration. Technique 9: Physical Constants of Solids: The Melting Point. Technique 10: Solubility. Technique 11: Crystallization: Purification of Solids. Technique 12: Extractions, Separations, and Drying Agents. Technique 13: Physical Constants of Liquids: The Boiling Point and Density. Technique 14: Simple Distillation. Technique 15: Fractional Distillation, Azeotropes. Technique 16: Vacuum Distillation, Manometers. Technique 17: Sublimation. Technique 18: Steam Distillation. Technique 19: Column Chromatography. Technique 20: Thin-Layer Chromatography. Technique 21: High- Performance Liquid Chromatography (HPLC). Technique 22: Gas Chromatography. Technique 23: Polarimetry. Technique 24: Refractometry. Technique 25: Infrared Spectroscopy. Technique 26: Nuclear Magnetic Resonance Spectroscopy. Technique 27: Carbon-13 Nuclear Magnetic Resonance Spectroscopy Technique 28: Mass Spectrometry. Technique 29: Guide to the Chemical Literature. APPENDICES: Appendix 1: Tables of Unknowns and Derivatives. Appendix 2: Procedures for Preparing Derivatives. Appendix 3: Index of Spectra. 2013, 1040pp, Paperback, 9781133107415 A SMALL SCALE APPROACH TO ORGANIC LABORATORY TECHNIQUES, 3E Donald L. Pavia, Western Washington University; Gary M. Lampman, Western Washington University; George S. Kriz, Western Washington University; Randall G. Engel, North Seattle Community College Featuring new experiments, a new essay, and new coverage of nanotechnology, this organic chemistry laboratory textbook offers a comprehensive treatment of laboratory techniques including small-scale and some microscale methods that use standard-scale ( macroscale ) glassware and equipment. The book is organized based on essays and topics of current interest and covers a large number of traditional organic reactions and syntheses, as well as experiments with a biological or health science focus. Seven introductory technique-based experiments, thirteen project-based experiments, and sections on green chemistry and biofuels spark students interest and engage them in the learning process. Instructors may choose to offer Cengage Learning s optional Premium Website, which contains videos on basic organic laboratory techniques. NEW TO THIS EDITION The Third Edition features a new essay, Biofuels, and two new experiments: Experiment 25, Biodiesel and Experiment 26, Ethanol from Corn. Nanotechnology is introduced with a new demonstration in Experiment 1 forming a selfassembled monolayer (SAM). Coverage of green chemistry is expanded and revised; and all new spectra are included in Technique 26 Nuclear Magnetic Resonance Spectroscopy (Proton NMR). An expanded section of project-based experiments now includes a new Experiment 64, Green Epoxidation of Chalcones and a new Experiment 65, Cyclopropanation Reactions on Chalcones. In all 85

of these experiments, students must either solve a significant problem or they must generate all or part of a procedure. Intended to promote critical thinking, these experiments not only challenge students, but also give them a feeling of what it is like to do research in chemistry. Instructors may choose to offer a new Premium Website that includes video demonstrations of key techniques in the book. Each of video has a series of questions with instant grading and feedback, so students can test their understanding of the TECHNIQUES and email their assessment results to their instructors. The textbook contains a variety of well-written, comprehensive, and pre-tested small-scale experiments using standard-scale (macroscale) glassware and equipment. Essays and examples on contemporary topics, such as biofuels and nanotechnology are provided to spark student interest and engage them in the learning process. Green chemistry is now better integrated due to its importance as a topic for students. Infrared, proton NMR, and 13C NMR spectroscopy is incorporated into many experiments. Some experiments also have an option to use gas chromatography-mass spectrometry. The authors include introductory, techniques-based experiments first to meet the needs of instructors who do not want to jump immediately into advanced material. Introduction. WELCOME TO ORGANIC CHEMISTRY. Laboratory Safety. Organization of the Textbook. Advance Preparation. Budgeting Time. Purpose. PART I: INTRODUCTION TO BASIC LABORATORY TECHNIQUES. Experiment 1. Solubility. Experiment 2. Crystallization. Experiment 3. Extraction. Experiment 4. A Separation and Purification Scheme. Experiment 4A. Extractions with a Separatory Funnel. Experiment 4B. Extractions with a Screw-Cap Centrifuge Tube Experiment 5. Chromatography. Experiment 5A. Thin- Layer Chromatography. Experiment 5B. Selecting the Correct Solvent for Thin-Layer Chromatography. Experiment 5C. Monitoring a Reaction with Thin Layer Chromatography. Experiment 5D. Column Chromatography. Experiment 6. Simple and Fractional Distillation Experiment 7. Infrared Spectroscopy and Boiling-Point Determination Essay. Aspirin. Experiment 8. Acetylsalicylic Acid. Essay. Analgesics. Experiment 9. Acetaminophen. Essay. Identification of Drugs. Experiment 10.TLC Analysis of Analgesic Drugs. Essay. Caffeine. Experiment 11. Isolation of Caffeine. Experiment 11A. Extraction of Caffeine from Tea. Experiment 11B. Isolation of Caffeine from a Tea Bag. Essay. Esters Flavors and Fragrances. Experiment 12: Isopentyl Acetate (Banana Oil). Essay, Terpenes and Phenylpropanoids. Experiment 13. Isolation of Eugenol from Cloves. Essay. Stereochemical Theory of Odor. Experiment 14. Spearmint and Caraway Oil: (+)- and (-)- Carvones. Essay.The Chemistry of Vision. Experiment 15. Isolation of Chlorophyll and Carotenoid Pigments from Spinach. Essay: Ethanol and Fermentation Chemistry. Experiment 16. Ethanol from Sucrose. PART II: INTRODUCTION TO MOLECULAR MODELING. Essay: Molecular Modeling and Molecular Mechanics. Experiment 17. An Introduction to Molecular Modeling. Experiment 17A. The Conformations of n-butane: Local Minima. Experiment 17B. Cyclohexane Chair and Boat Conformations. Experiment 17C. Substituted Cyclohexane Rings (Critical Thinking Exercise). Experiment 17D. cis- and trans-2-butene. Essay: Computational Chemistry - Ab initio and Semiempirical Methods. Experiment 18. Computational Chemistry. Experiment 18A. Heats of Formation: Isomerism, Tautomerism, and Regioselectivity. Experiment 18B. Heats of Reactions: SN1 Reaction Rates. Experiment 18C. Density-Electrostatic Potential. Maps: Acidities of Carboxylic Acids. Experiment 18D. Density -Electrostatic Potential Maps: Carbocations. Experiment 18E. Density -LUMO Maps: Reactivities of Carbonyl Groups. PART III: PREPARATIONS AND REACTIONS OF ORGANIC COMPOUNDS. Experiment 19. Reactivities of Some Alkyl Halides. Experiment 20. Nucleophilic Substitution Reactions: Competing Nucleophiles. Experiment 20A. Competing Nucleophiles with 1-Butanol or 2-Butanol. Experiment 20B. Competing Nucleophiles with 2-Methyl-2-Propanol. Experiment 20C. Analysis. Experiment 21. Synthesis of n-butyl Bromide and t-pentyl Chloride. Experiment 21A. n-butyl Bromide. Experiment 21B. t-pentyl Chloride. Experiment 22. 4-Methylcyclohexene Essay. Fats and Oils. Experiment 86

23. Methyl Stearate from Methyl Oleate. Essay: Petroleum and Fossil Fuels. Experiment 24. Gas Chromatographic Analysis of Gasolines. Essay: Biofuels. Experiment 25. Biodiesel. Experiment 25A. Biodiesel from Coconut Oil. Experiment 25B. Biodiesel from Other Oils. Experiment 25C. Analysis of Biodiesel. Experiment 26. Ethanol from Corn. Essay: Green Chemistry. Experiment 27. Chiral Reduction of Ethyl Acetoacetate; Optical Purity Determination. Experiment 27A. Chiral Reduction of Ethyl Acetoacetate. Experiment 27B. NMR Determination of the Optical Purity of Ethyl (S)-3- Hydroxybutanoate. Experiment 28. Nitration of Aromatic Compounds Using a Recyclable Catalyst. Experiment 29. Reduction of Ketones Using Carrots as Biological Reducing Agents Experiment 30. Resolution of (+/-)-alpha-phenylethylamine and Determination of Optical Purity. Experiment 30A. Resolution of (+/-)-alpha-phenylethylamine. Experiment 30B. Determination of Optical Purity Using NMR and a Chiral Resolving Agent. Experiment 31. An Oxidation- Reduction Scheme: Borneol, Camphor, Isoborneol. Experiment 32. Multistep Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid. Experiment 32A. Preparation of Benzoin by Thiamine Catalysis. Experiment 32B. Preparation of Benzil. Experiment 32C. Preparation of Benzilic Acid. Experiment 33. Triphenylmethanol and Benzoic Acid. Experiment 33A. Triphenylmethanol. Experiment 33B. Benzoic Acid. Experiment 34. Aqueous-Based Organozinc Reactions. Experiment 35. Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes Using a Palladium Catalyst. Experiment 36. Grubbs Catalyzed Metathesis of Eugenol with 1,4-Butenediol to Prepare a Natural Product. Experiment 37. The Aldol Condensation Reaction: Preparation of Benzalacetophenones (Chalcones). Experiment 38. A Green Enantioselective Aldol Condensation Reaction. Experiment 39. Preparation of an Unsaturated Ketone via Michael and Aldol Condensation Reactions. Experiment 40. Preparation of Triphenylpyridine. Experiment 41. 1,4-Diphenyl-1,3-Butadiene. Experiment 42. Relative Reactivities of Several Aromatic Compounds. Experiment 43. Nitration of Methyl Benzoate. Essay. Local Anesthetics. Experiment 44. Benzocaine. Essay. Pheromones: Insect Attractants and Repellants. Experiment 45. N,N-Diethyl-m-toluamide: The Insect Repellent OFF. Essay: Sulfa Drugs. Experiment 46. Sulfa Drugs: Preparation of Sulfanilamide. Essay: Polymers and Plastics. Experiment 47. Preparation and Properties of Polymers: Polyester, Nylon, and Polystyrene. Experiment 47A. Polyesters. Experiment 47B. Polyamide (Nylon). Experiment 47C. Polystyrene. Experiment 47D. Infrared Spectra of Polymer Samples. Experiment 48. Ring-Opening Metathesis Polymerization (ROMP) Using a Grubbs Catalyst: A Three Step Synthesis of a Polymer. Experiment 48A. Diels-Alder Reaction of Furan and Maleic Anhydride. Experiment 48B. Ring Opening of Anhydride in Methanol. Experiment 48C. Ring-Opening Metathesis Polymerization (ROMP). Experiment 49. Diels-Adler Reaction Experiment 49A. Conversion of the Diels-Adler Adduct to the Diester Experiment 49B. Synthesizing the Polymer by Ring- Opening Metathesis Polymerization (ROMP) Essay. Diels Alder Reaction and Insecticides. Experiment 50. The Diels Alder Reaction of Cyclopentadiene with Maleic Anhydride. Experiment 51. Diels-Adler Reaction with Anthracine-9-Methanol. Experiment 52. Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. Experiment 52A. Photoreduction of Benzophenone. Experiment 52B. Synthesis of Benzopinacolone: The Acid-Catalyzed Rearrangement of Benzpinacol. Essay. Fireflies and Photochemistry. Experiment 53. Luminol. Essay. The Chemistry of Sweeteners. Experiment 54. Carbohydrates. Experiment 55. Analysis of a Diet Soft Drink by HPLC. Part IV: IDENTIFICATION OF ORGANIC SUBSTANCES. Experiment 56. Identification of Unknowns. Experiment 56A. Solubility Tests. Experiment 56B. Tests for the Elements (N, S, X). Experiment 56C. Tests for Unsaturation. Experiment 56D. Aldehydes and Ketones. Experiment 56E. Carboxylic Acids. Experiment 56F. Phenols. Experiment 56G. Amines. Experiment 56H. Alcohols. Experiment 56I. Esters. PART V: PROJECT- BASED EXPERIMENTS. Experiment 57. Preparation of a C-4 or C-5 Acetate Ester. Experiment 58. Isolation of Essential Oils from Allspice, Caraway, Cinnamon, Cloves, Cumin, Fennel, or Star Anise. Experiment 58A. Isolation of Essential Oils by Steam Distillation. Experiment 58B. Identification of the Constituents of Essential Oils by Gas Chromatography-Mass Spectrometry. Experiment 58C. Investigation of the Essential Oils of Herbs and Spices-Mini-Research Project. Experiment 59. Competing Nucleophiles in SN1 and SN2 Reactions: Investigations Using 2-Pentanol and 3-Pentanol. 87

Experiment 60. Friedel-Crafts Acylation. Experiment 61. The Analysis of Antihistamine Drugs by Gas Chromatography-Mass Spectrometry. Experiment 62. Carbonation of an Unknown Aromatic Halide. Experiment 63. The Aldehyde Enigma. Experiment 64. Synthesis of Substituted Chalcones: A Guided-Inquiry Experience. Experiment 65. Green Epoxidation of Chalcones. Experiment 66: Cyclopropanation Reactions of Chalcones. Experiment 67. Michael and Aldol Condensation Reactions. Experiment 68. Esterification Reactions of Vanillin: The Use of NMR to Solve a Structure Proof Problem. Experiment 69. An Oxidation Puzzle. PART VI: THE TECHNIQUES. Technique 1. Laboratory Safety. Technique 2. The Laboratory Notebook, Calculations, and Laboratory Records. Technique 3. Laboratory Glassware: Care and Cleaning. Technique 4. How to Find Data for Compounds: Handbooks and Catalogues. Technique 5. Measurement of Volume and Weight. Technique 6. Heating and Cooling Methods. Technique 7. Reaction Methods. Technique 8. Filtration. Technique 9. Physical Constants of Solids: The Melting Point. Technique 10. Solubility. Technique 11. Crystallization: Purification of Solids. Technique 12. Extractions, Separations, and Drying Agents. Technique 13. Physical Constants of Liquids: The Boiling Point and Density. Technique 14. Simple Distillation. Technique 15. Fractional Distillation, Azeotropes. Technique 16. Vacuum Distillation, Manometers. Technique 17. Sublimation. Technique 18. Steam Distillation. Technique 19. Column Chromatography. Technique 20. Thin-Layer Chromatography. Technique 21. High-Performance Liquid Chromatography (HPLC). Technique 22. Gas Chromatography. Technique 23. Polarimetry. Technique 24. Refractometry. Technique 25. Infrared Spectroscopy. Technique 26. Nuclear Magnetic Resonance Spectroscopy (Proton NMR). Technique 27. Carbon-13 Nuclear Magnetic Resonance Spectroscopy. Technique 28. 6 Mass Spectrometry. Technique 29. Guide to the Chemical Literature. Appendix 1: Tables of Unknowns and Derivatives. Appendix 2: Procedure for Preparing Derivatives. Appendix 3: Index of Spectra. CHEMICAL PRINCIPLES FOR ORGANIC CHEMISTRY Robert Boikess, Rutgers, the State University of New Jersey To help students succeed in the much tougher and more rigorous Organic Chemistry class, CHEMICAL PRINCIPLES FOR ORGANIC CHEMISTRY presents all of the necessary topics from General Chemistry in the way that organic chemists use them. The book helps students unlearn some of the approaches they learned in General Chemistry, learn new or different ones, and successfully apply concepts from General Chemistry to Organic Chemistry. This relatively short ancillary text presents all of the necessary topics from General Chemistry in the way organic chemists use them. This book greatly simplifies the task of getting students up to speed in the Organic Chemistry course by teaching them how to apply concepts from General Chemistry to Organic Chemistry. 1. Valence Bond Theory. 2. Molecular Orbital Theory. 3. Acids and Bases. 4. Thermochemistry and Thermodynamics. 5. Chemical Kinetics. 2015, 224pp, Paperback, 9781285457697 2011, 1024pp, Hardback, 9781439049327 88

EXPERIMENTAL ORGANIC CHEMISTRY, 5E A Miniscale and Microscale Approach, International Edition Stephen F. Martin, University of Texas at Austin; John C. Gilbert, Santa Clara Univerisity Providing even more emphasis on inquiry-based learning, a new green experiment, and more than a dozen new discovery experiments, this Fifth Edition of Martin and Gilbert s proven Organic Chemistry Lab Experiments: Miniscale & Microscale, International Edition contains procedures for both miniscale (also known as small scale) and microscale users. The manual first covers equipment, record keeping, and safety in the laboratory, then walks students step by step through the laboratory techniques they need to perform the book s experiments with confidence. Chapters show students how to use the book s techniques to synthesize compounds and analyze their properties, complete multi-step syntheses of organic compounds, and solve structures of unknown compounds. A bioorganic experiment in Chapter 24 reflects the increasing emphasis on bioorganic chemistry in the course and gives students an opportunity to accomplish a mechanistically interesting and synthetically important coupling of two a-amino acids to produce a dipeptide. NEW TO THIS EDITION This edition places even more emphasis on inquirybased learning, with more than a dozen new discovery experiments. The fifth edition includes new and updated Historical Highlights on Polymorphs, Performance Enhancing Drugs, Acetylene, and Chiral Drugs. Offers a new green experiment on the Bromination of (E)-Stilbene. Includes video demonstrations of key techniques in the book in an optional new Premium Companion Website. The website also contains pre-lab exercises, proton NMR spectra for analyzing chemical shifts, integration, and coupling constants, IR spectra for analyzing functional groups, MSDS (material safety data sheets) tables for checking the safe handling of the materials in each experiment, and derivative tables. Emphasizes safety through Safety Alerts and Wrapping It Up sections that alert students to possible hazards and proper disposal of spent chemicals. Includes fascinating Historical Highlights, brief essays that familiarize students with the lives of chemical pioneers who have advanced the field of chemistry. Includes accurately drawn art to show students how to set up an experiment with confidence. Includes margin drawings of equipment to remind students about the set up for such techniques as distillation and reflux. This book helps students understand laboratory techniques by beginning each experiment with a thorough discussion of the theory and procedures involved and laying out experimental procedures in a clear format. 1. Laboratory Overview. 2. Techniques and Apparatus. 3. Recrystallization and Melting Points. 4. Distillation and Boiling Points. 5. Extraction. 6. Chromatography. 7. Stereochemistry. 8. Spectral Methods. 9. Alkanes. 10. Alkenes. 11. Alkynes. 12. Dienes and the Diels-Alder Reaction. 13. Kinetic and Thermodynamic Control of a Reaction. 14. Nucleophilic Substitution 451. 15. Electrophilic Aromatic Substitution. 16. Oxidation 525. 17. Reduction. 18. Carbonyl Compounds 585. 19. Organometallic Chemistry. 20. Carboxylic Acids and Their Derivatives. 21. Multistep Synthesis. 22. Polymers. 23. Carbohydrates. -Amino Acids and Peptides. 24. 25. Identifying Organic Compounds. 26. The Literature of Organic Chemistry. 2011, 960pp, Paperback, 9781439049167 89

FUNDAMENTALS OF ORGANIC CHEMISTRY, INTERNATIONAL EDITION, 7E John E. McMurry, Cornell University Retaining the concise, to-the-point presentation that has already helped thousands of students move beyond memorization to a true understanding of the beauty and logic of organic chemistry, this Seventh Edition of John McMurry s FUNDAMENTALS OF ORGANIC CHEMISTRY brings in new, focused content that shows students how organic chemistry applies to their everyday lives. In addition, redrawn chemical structures and artwork help students visualize important chemical concepts, a greater emphasis on biologically-related chemistry (including new problems) helps them grasp the enormous importance of organic chemistry in understanding the reactions that occur in living organisms, and new EOC problems keyed to OWL allow them to work text-specific problems online. Finally, for this edition, John McMurry reevaluated and revised his writing at the sentence level to ensure that the book s explanations, applications, and examples are more student-friendly, relevant, and motivating than ever before. NEW TO THIS EDITION The problem sets now include additional biologicallyoriented problems in most chapters, shortened and focused In the Medicine Cabinet and In the Field end-of-chapter problems, and new End of Chapter problems keyed to OWL that match the text to online homework. Redrawn art and chemical structures (as well as computer-generated Orbitals) help students visualize chemistry processes and structures. Titles have been added to Worked Examples to provide students with a frame of reference. New Why This Chapter? explanations in chapter introductions explain the relevance of chapter material to students. The book s writing has been revised at the sentence level to make the presentation even more studentfriendly, relevant, and motivating. Clear explanations, thought-provoking examples, and an innovative vertical format for explaining reaction mechanisms make the text relevant and studentfriendly. Applied chapter openers with associated photos and molecular models help students see the relevance of chapter content. The text s full color presentation highlights the reacting parts of molecules and uses computergenerated ball-and-stick molecular models to aid students three-dimensional perception. Nearly 100 electrostatic potential maps display the polarity patterns in molecules and the importance of these patterns in determining chemical reactivity. 1. Structure and Bonding; Acids and Bases. 2. The Nature of Organic Compounds: Alkanes. 3. The Nature of Organic Reactions: Alkenes. 4. Reactions of Alkenes and Alkynes. 5. Aromatic Compounds. 6. Stereochemistry. 7. Alkyl Halides. 8. Alcohols, Phenols, and Ethers. 9. Aldehydes and Ketones: Nucleophilic Addition Reactions. 10. Carboxylic Acids and Derivatives. 11. Carbonyl Alpha-Substitution Reactions and Condensation Reactions. 12. Amines. INTERLUDE: THE ROADMAP OF CHEMICAL REACTIONS. 13. Structure Determination. 14. Biomolecules: Carbohydrates. 15. Biomolecules: Amino Acids, Peptides, and Proteins. 16. Biomolecules: Lipids and Nucleic Acids. 17. The Organic Chemistry of Metabolic Pathways. 2011, 672pp, Paperback, 9781439049730 90

INTRODUCTION TO ORGANIC LABORATORY TECHNIQUES, 3E A Small-Scale Approach, International Edition Randall G. Engel, North Seattle Community College; George S. Kriz, Western Washington University; Gary M. Lampman, Western Washington University; Donald L. Pavia, Western Washington University Featuring new experiments, a new essay, and new coverage of nanotechnology, this organic chemistry laboratory textbook offers a comprehensive treatment of laboratory techniques including small-scale and some microscale methods that use standard-scale ( macroscale ) glassware and equipment. The book is organized based on essays and topics of current interest and covers a large number of traditional organic reactions and syntheses, as well as experiments with a biological or health science focus. Seven introductory technique-based experiments, thirteen project-based experiments, and sections on green chemistry and biofuels spark students interest and engage them in the learning process. Instructors may choose to offer Cengage Learning s optional Premium Website, which contains videos on basic organic laboratory techniques. NEW TO THIS EDITION The Third Edition features a new essay, Biofuels, and two new experiments: Experiment 25, Biodiesel and Experiment 26, Ethanol from Corn. Nanotechnology is introduced with a new demonstration in Experiment 1 forming a selfassembled monolayer (SAM). Coverage of green chemistry is expanded and revised; and all new spectra are included in Technique 26 Nuclear Magnetic Resonance Spectroscopy (Proton NMR). An expanded section of project-based experiments now includes a new Experiment 64, Green Epoxidation of Chalcones and a new Experiment 65, Cyclopropanation Reactions on Chalcones. In all of these experiments, students must either solve a significant problem or they must generate all or part of a procedure. Intended to promote critical thinking, these experiments not only challenge students, but also give them a feeling of what it is like to do research in chemistry. The textbook contains a variety of well-written, comprehensive, and pre-tested small-scale experiments using standard-scale (macroscale) glassware and equipment. Essays and examples on contemporary topics, such as biofuels and nanotechnology are provided to spark student interest and engage them in the learning process. Green chemistry is now better integrated due to its importance as a topic for students. Infrared, proton NMR, and 13C NMR spectroscopy is incorporated into many experiments. Some experiments also have an option to use gas chromatography-mass spectrometry. The authors include introductory, techniques-based experiments first to meet the needs of instructors who do not want to jump immediately into advanced material. Introduction. WELCOME TO ORGANIC CHEMISTRY. Laboratory Safety. Organization of the Textbook. Advance Preparation. Budgeting Time. Purpose. Part One: The Techniques. Technique 1: Laboratory Safety. Technique 2: The Laboratory Notebook, Calculations, and Laboratory Records. Technique 3: Laboratory Glassware: Care and Cleaning. Technique 4: How to Find Data for Compounds: Handbooks and Catalogs. Technique 5: Measurement of Volume and Weight. Technique 6: Heating and Cooling Methods. Technique 7: Reaction Methods. Technique 8: Filtration. Technique 9: Physical Constants of Solids: The Melting Point. Technique 10: Solubility. Technique 11: Crystallization: Purification of Solids. Technique 12: Extractions, Separations, and Drying Agents. Technique 13: Physical Constants of Liquids: The Boiling Point and Density. Technique 14: Simple Distillation. Technique 15: Fractional Distillation, Azeotropes. Technique 16: 91

Vacuum Distillation, Manometers. Technique 17: Sublimation. Technique 18: Steam Distillation. Technique 19: Column Chromatography. Technique 20: Thin-Layer Chromatography. Technique 21: High-Performance Liquid Chromatography (HPLC). Technique 22: Gas Chromatography. Technique 23: Polarimetry. Technique 24: Refractometry. Technique 25: Infrared Spectroscopy. Technique 26: Nuclear Magnetic Resonance Spectroscopy (Proton NMR). Technique 27: Carbon-13 Nuclear Magnetic Resonance Spectroscopy. Technique 28: 6 Mass Spectrometry. Technique 29: Guide to the Chemical Literature. Part Two: Introduction to Basic Laboratory Techniques. Experiment 1: Solubility. Experiment 2: Crystallization. Experiment 3: Extraction. Experiment 4: A Separation and Purification Scheme. Experiment 4A: Extractions with a Separatory Funnel. Experiment 5: Chromatography. Experiment 5A: Thin- Layer Chromatography. Experiment 5B: Selecting the Correct Solvent for Thin-Layer Chromatography. Experiment 5C: Monitoring a Reaction with Thin Layer Chromatography. Experiment 5D: Column Chromatography. Experiment 6: Simple and Fractional Distillation. Experiment 7: Infrared Spectroscopy and Boiling-Point Determination. Experiment 8: Acetylsalicylic Acid. Experiment 9: Acetaminophen. Experiment 10: TLC Analysis of Analgesic Drugs. Experiment 11: Isolation of Caffeine. Experiment 11A: Extraction of Caffeine from Tea. Experiment 11B: Isolation of Caffeine from a Tea Bag. Experiment 12: Isopentyl Acetate (Banana Oil). Experiment 13: Isolation of Eugenol from Cloves. Experiment 14: Spearmint and Caraway Oil: (+)- and (-)-Carvones. Experiment 15: Isolation of Chlorophyll and Carotenoid Pigments from Spinach. Experiment 16: Ethanol from Sucrose. Part Three: Introduction to Molecular Modeling. Experiment 17: An Introduction to Molecular Modeling. Experiment 17A: The Conformations of n-butane: Local Minima. Experiment 17B: Cyclohexane Chair and Boat Conformations. Experiment 17C: Substituted Cyclohexane Rings (Critical Thinking Exercise). Experiment 17D: cis- and trans-2-butene. Experiment 18: Computational Chemistry. Experiment 18A: Heats of Formation: Isomerism, Tautomerism, and Regioselectivity. Experiment 18B: Heats of Reaction: SN1 Reaction Rates. Experiment 18C: Density Electrostatic Potential Maps: Acidities of Carboxylic Acids. Experiment 18D: Density Electrostatic Potential Maps: Carbocations. Experiment 18E: Density LUMO Maps: Reactivities of Carbonyl Groups. Part Four: Preparations and Reactions of Organic Compounds. Experiment 19: Reactivities of Some Alkyl Halides. Experiment 20: Nucleophilic Substitution Reactions: Competing Nucleophiles. Experiment 20A: Competitive Nucleophiles with 1-Butanol or 2-Butanol. Experiment 20B: Competitive Nucleophiles with 2-Methyl-2-Propanol. Experiment 20C: Analysis. Experiment 21: Synthesis of n-butyl Bromide and t-pentyl Chloride. Experiment 21A: n-butyl Bromide. Experiment 21B: t-pentyl Chloride. Experiment 22: 4-Methylcyclohexene. Experiment 23: Methyl Stearate from Methyl Oleate. Experiment 24: Gas- Chromatographic Analysis of Gasolines. Experiment 25: Biodiesel. Experiment 25A: Biodiesel from Coconut Oil. Experiment 25B: Biodiesel from Other Oils. Experiment 25C: Analysis of Biodiesel. Experiment 26: Ethanol from Corn. Experiment 27: Chiral Reduction of Ethyl Acetoacetate; Optical Purity Determination. Experiment 27A: Chiral Reduction of Ethyl Acetoacetate. Experiment 27B: NMR Determination of the Optical Purity of Ethyl (S)-3-Hydroxybutanoate. Experiment 28: Nitration of Aromatic Compounds Using a Recyclable Catalyst. Experiment 29: Reduction of Ketones Using Carrots as Biological Reducing Agents. Experiment 30: Resolution of (±)-a-phenylethylamine and Determination of Optical Purity. Experiment 30A: Resolution of (±)-a-phenylethylamine. Experiment 30B: Determination of Optical Purity Using NMR and a Chiral Resolving Agent. Experiment 31: An Oxidation-Reduction Scheme: Borneol, Camphor, Isoborneol. Experiment 32: Multistep Reaction Sequences: The Conversion of Benzaldehyde to Benzilic Acid. Experiment 32A: Preparation of Benzoin by Thiamine Catalysis. Experiment 32B: Preparation of Benzil. Experiment 32C: Preparation of Benzilic Acid. Experiment 33: Triphenylmethanol and Benzoic Acid. Experiment 33A: Triphenylmethanol. Experiment 33B: Benzoic Acid. Experiment 34: Aqueous-Based Organozinc Reactions. Experiment 35: Sonogashira Coupling of Iodosubstituted Aromatic Compounds with Alkynes using a Palladium Catalyst. Experiment 36: Grubbs Catalyzed Metathesis of Eugenol with 1,4-Butenediol to Prepare a Natural Product. Experiment 37: The Aldol 92

Condensation Reaction: Preparation of Benzalacetophenones (Chalcones). Experiment 38: A Green Enantioselective Aldol Condensation Reaction. Experiment 39: Preparation of an a,b-unsaturated Ketone via Michael and Aldol Condensation Reactions. Experiment 40: Preparation of Triphenylpyridine. Experiment 41: 1,4-Diphenyl-1,3-Butadiene. Experiment 42: Relative Reactivities of Several Aromatic Compounds. Experiment 43: Nitration of Methyl Benzoate. Experiment 44: Benzocaine. Experiment 45: N,N-Diethyl-mtoluamide: The Insect Repellent OFF. Experiment 46: Sulfa Drugs: Preparation of Sulfanilamide. Experiment 47: Preparation and Properties of Polymers: Polyester, Nylon, and Polystyrene. Experiment 49A: Polyesters. Experiment 49B: Polyamide (Nylon). Experiment 49C: Polystyrene. Experiment 49D: Infrared Spectra of Polymer Samples. Experiment 48: Ring-Opening Metathesis Polymerization (ROMP) Using a Grubbs Catalyst: A Three-Step Synthesis of a Polymer. Experiment 48A: Diels-Alder Reaction of Furan and Maleic Anhydride. Experiment 48B: Ring Opening of Anhydride in Methanol. Experiment 48C: Ring-Opening Metathesis Polymerization (ROMP). Experiment 48A: Diels-Adler Reaction. Experiment 48B: Conversion of the Diels-Adler Adduct to the Diester. Experiment 48C: Synthesizing the Polymer by Ring-Opening Metathesis Polymerization (ROMP). Experiment 49: The Diels Alder Reaction of Cyclopentadiene with Maleic Anhydride. Experiment 50: Diels-Alder Reaction with Anthracene- 9-methanol. Experiment 51: Photoreduction of Benzophenone and Rearrangement of Benzpinacol to Benzopinacolone. Experiment 51A: Photoreduction of Benzophenone. Experiment 51B: Synthesis of b-benzpinacolone: The Acid-Catalyzed Rearrangement of Benzpinacol. Experiment 52: Luminol. Experiment 53: Analysis of A Diet Soft Drink by HPLC. Experiment 54: Carbohydrates. Part Four: Identification of Organic Substances. Experiment 55: Identification of Unknowns. Experiment 55A: Solubility Tests. Experiment 55B: Tests of the Elements (N, S, X). Experiment 55C: Tests for Unsaturation. Experiment 55D: Aldehydes and Ketones. Experiment 55E: Carboxylic Acids. Experiment 55F: Phenols. Experiment 55G: Amines. Experiment 55H: Alcohols. Experiment 55I: Esters. Part Six: Project-Based Experiments. Experiment 56: Preparation of a C-4 or C-5 Acetate Ester. Experiment 57: Isolation of Essential Oils from Allspice, Caraway, Cinnamon, Cloves, Cumin, Fennel, or Star Anise. Experiment 57A: Isolation of Essential Oils by Steam Distillation. Experiment 57B: Identification of the Constituents of Essential Oils by Gas Chromatography Mass Spectrometry. Experiment 57C: Investigation of the Essential Oils of Herbs and Spices A Mini-Research Project. Experiment 58: Competing Nucleophiles in SN1 and SN2 Reactions: Investigations Using 2-Pentanol and 3-Pentanol. Experiment 59: Friedel Crafts Acylation. Experiment 60: The Analysis of Antihistamine Drugs by Gas Chromatography Mass Spectrometry. Experiment 61: Carbonation of an Unknown Aromatic Halide. Experiment 62 The Aldehyde Enigma. Experiment 63 Synthesis of Substituted Chalcones: A Guided-Inquiry Experience. Experiment 64: Green Epoxidation of Chalcones. Experiment 65: Cyclopropanation Reactions on Chalcones. Experiment 66: Michael and Aldol Condensation Reactions. Experiment 67: Esterification Reactions of Vanillin: The Use of NMR to Determine at Structure. Experiment 68: An Oxidation Puzzle. Part Seven: Essays. Essay 1: Aspirin. Essay 2: Analgesics. Essay 3: Identification of Drugs. Essay 4: Caffeine. Essay 5: Esters Flavors and Fragrances. Essay 6: Terpenes and Phenylpropanoids. Essay 7: Stereochemical Theory of Odor. Essay 8: The Chemistry of Vision. Essay 9: Ethanol and Fermentation Chemistry. Essay 10: Molecular Modeling and Molecular Mechanics. Essay 11: Computational Chemistry ab Intio and Semiempirical Methods. Essay 12: Fats and Oils. Essay 13: Petroleum and Fossil Fuels. Essay 14: Biofuels. Essay 15: Green Chemistry. Essay 16: Local Anesthetics. Essay 17: Pheromones: Insect Attractants. Essay 18: Sulfa Drugs. Essay 19: Polymers and Plastics. Essay 20: Diels-Alder Reaction and Insecticides. Essay 21: Fireflies and Photochemistry. Essay 22: The Chemistry of Sweeteners. Appendices. Appendix 1: Tables of Unknowns and Derivatives. Appendix 2: Procedures for Preparing Derivatives. Appendix 3 Index of Spectra. 2011, 1024pp, Paperback, 9780538733281 93

MACROSCALE AND MICROSCALE ORGANIC EXPERIMENTS, 6E Kenneth L. Williamson, Mount Holyoke College, Emeritus; Katherine M. Masters, Pennsylvania State University The market leader for the full-year organic laboratory, this manual derives many experiments and procedures from the classic Feiser lab text, giving it an unsurpassed reputation for solid, authoritative content. The Sixth Edition includes new experiments that stress greener chemistry, as well as updated NMR spectra and a Premium Website that includes glassware-specific videos with pre-lab, gradable exercises. Offering a flexible mix of macroscale and microscale options for most experiments, this proven manual emphasizes safety and allows instructors to save on the purchase and disposal of expensive, sometimes hazardous, organic chemicals. Macroscale versions can be used for less costly experiments, allowing students to get experience working with conventionally-sized glassware. NEW TO THIS EDITION UPDATED NMR SPECTRA. The authors have fully updated NMR spectra throughout the manual. NEW AND UPDATED LABS AND EXPERIMENTS. Many labs have been updated, and new lab experiments include A Diels-Alder Reaction Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride and Multicomponent Reactions: The Aqueous Passerini Reaction, and Virstatin, a Possible Treatment for Cholera. PREMIUM WEBSITE. A new Premium Website includes glassware-specific videos with pre-lab, gradable exercises. GREENER CHEMISTRY. Experiments that stress greener chemistry appear throughout the manual and are identified with a green chemistry icon. For example, the use of household bleach is explored as an alternative to the toxic chromium ion as an oxidizing agent for cyclohexanol. AN EMPHASIS ON LABORATORY SAFETY. The laboratory safety chapter includes material on working with closed systems and laboratory courtesy. A STRONG MASS SPECTROMETRY CHAPTER. The chapter on mass spectrometry describes time-offlight and mass quadrupole analyzers and includes sections on GC-MS and computer-aided spectral identification, as well as ESI and MALDI ionization. BIOASSAY EXPERIMENTS. The manual s bioassay experiments include a bioassay of eugenol isolated from cloves. COMPREHENSIVE COVERAGE. Material is offered on diffuse reflectance IR analysis, capillary GC, and temperature programming. 1. Introduction. 2. Laboratory Safety, Courtesy, and Waste Disposal Techniques. 3. Melting Points and Boiling Points. 4. Recrystallization. 5. Distillation. 6. Steam Distillation, Vacuum Distillation, and Sublimation. 7. Extraction. 8. Thin-Layer Chromatography: Analysis of Analgesics and Isolating Lycopene from Tomato Paste. 9. Column Chromatography: Fluorenone, Cholesteryl Acetate, Acetylferrocene, and Plant Pigments. 10. Gas Chromatography: Analysis of Alkene Isomers. 11. Infrared Spectroscopy. 12. Nuclear Magnetic Resonance Spectroscopy. 13. Mass Spectroscopy. 14. Ultraviolet Spectroscopy, Refractive Indices, and Qualitative Instrumental Organic Analysis. 15. Computational Chemistry Elimination, Substitution, and Addition. 16. The SN2 Reaction: 1-Bromobutane. 17. Nucleophilic Substitution Reactions of Alkyl Halides. 18. Radical Initiated Chlorination of 1-Chlorobutane. 19. Alkenes from Alcohols: Cyclohexene from Cyclohexanol. 20. Bromination and Debromination: Purification of Cholesterol. 21. Dichlorocarbene Oxidation and Reduction. 22. Oxidation: Cyclohexanol to Cyclohexanone; Cyclohexanone to Adipic Acid. 23. The Cannizzaro Reaction: Simultaneous Synthesis of an Alcohol and an Acid in the Absence of Solvent. 24. Oxidative Coupling of Alkynes: 2,7-Dimethyl-3,5-octadiyn-2,7-diol. 25. Catalytic Hydrogenation. 26. Sodium Borohydride Reduction of 2-Methylcyclohexanone: A Problem in Conformational Analysis. 27. Epoxidation of Cholesterol. Aromatic 94

Substitution and Elimination. 28. Nitration of Methyl Benzoate 29. Friedel-Crafts Alkylation of Benzene and Dimethoxybenzene; Host-Guest Chemistry. 30. Alkylation of Mesitylene. 31. The Friedel-Crafts Reaction: Anthraquinone and Anthracene. 32. Friedel- Crafts Acylation of Ferrocene: Acetylferrocene. 33. Reactions of Triphenylmethyl Carbocation, Carbanion, and Radical. 34. 1,2,3,4-Tetraphenylnaphthalene via Benzyne. 35. Triptycene via Benzyne Reactions of Aldehydes and Ketones. 36. Aldehydes and Ketones. 37. Dibenzalacetone by the Aldol Condensation. 38. Grignard Synthesis of Triphenylmethanol and Benzoic Acid. 39. The Wittig and Wittig-Horner Reactions Reactions of Carboxylic Acids, Esters, and Amines. 40. Esterification and Hydrolysis. 41. Acetylsalicylic Acid (Aspirin). 42. Malonic Ester of a Barbiturate. 43. Amines. 44. The Sandmeyer Reaction: 1-Bromo-4-chlorobenzene, 2-Iodobenzoic Acid, and 4-Chlorotoluene. 45. Synthesis and Bioessay of Sulfanilamide and Derivatives. 46. Dyes and Dyeing. 47. Martius Yellow. 48. Diels-Alder Reaction. 49. Ferrocene [Bis(cyclopentadienyl)iron]. 50. A Diels-Alder Reaction Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride. 51. Tetraphenylcyclopentadienone. 52. Hexaphenylbenzene and Dimethyl Tetraphenylphthalate. Derivatives of 1,2-Diphenylethane: A Multistep Synthesis. 53. The Benzoin Condensation: Catalysis by the Cyanide Ion and Thiamine. 54. Nitric Acid Oxidation; Preparation of Benzil from Benzoin; and Synthesis of a Heterocycle: Diphenylquinoxaline. 55. Borohydride Reduction of a Ketone: Hydrobenzoin from Benzil. 56. The Synthesis of 2,2-Dimethyl-1,5-dioxolane; The Acetonide Derivative of a Vicinal Diol. 57. The 1,4-Addition: Reductive Acetylation of Benzil. 58. Synthesis of an Alkyne from an Alkene; Bromination and Dehydrobromination: Stilbene and Diphenylacetylene. 59. The Perkin Reaction: Synthesis of a-phenylcinnamic Acid. 60. Multicomponent Reactions: The Aqueous Passerini Reaction. 61. Chemiluminescence: Syntheses of Cyalume and Luminol. 62. Photochemistry: The Synthesis of Benzopinacol Natural Product Chemistry and Biochemistry. 63. Carbohydrates and Sweeteners. 64. Virstatin, a Possible Treatment for Cholera. 65. Biosynthesis of Ethanol and Enzymatic Reactions. 66. The Synthesis of Natural Products: Pseudopellitierene and Camphor. 67. Polymers: Synthesis and Recycling. 68. Searching the Chemical Literature. 2011, 816pp, Hardback, 9780538733335 ORGANIC CHEMISTRY, 2E A Guided Inquiry Andrei Straumanis, College of Charleston Designed for use as a supplement to a traditional text to encourage active and collaborative learning in the classroom, this activity book incorporates new methods for teaching chemistry that reflect current research on how students learn. The purpose of the guided inquiry approach is to teach you to think analytically and collaboratively in teams, like scientists do, rather than teaching you to memorize important conclusions arrived at by great scientists of the past. By looking carefully at new problems, constructing logical conclusions based on observations, and discussing the merits of your conclusions with peers, you ll develop a stronger conceptual understanding of and appreciation for the material. Honing your logical and empirical skills enables you to better pursue not only chemistry, but any other complex sets of ideas. Unique ChemActivities not found in other texts and study guides consist of a series of Models, Critical Thinking Questions, and Skill Development Exercises that guide student groups in their exploration of organic chemistry. These materials introduce flexibility into a curriculum, enabling instructors to replace a lecture with group work on a ChemActivity. Students work in small groups while the instructor facilitates and leads whole-class discussions. Students deepen their scientific understanding by explaining topics to one another. Scientific Models are presented throughout the chapters in bulleted and illustrated formats, assisting conceptual learning. Critical Thinking Questions appear after each Model 95

and ask students to explore the ideas presented in a number of ways, including drawing a molecule, completing a table, or writing an explanation about a topic to another student who missed class that day. This multi-faceted approach addresses different learning styles, reinforces concepts, and can help reveal areas of weak understanding. Exercises following each Model and set of Critical Thinking Questions are matched to certain models presented in the chapter, and test students ability to solve problem based on that model. Intro Organic Chemistry: a Guided Inquiry. 1. Bond Angles and Shape. 2. Lewis Structures. 3. Electron Orbitals. 4. Polar Bonds, Polar Reactions. 5. Resonance. 6. Alkanes & Alkenes. 7. Cycloalkanes. 8. Addition via Carbocation. 9. Addition via Cyclic Intermediate. 10. Oxidation and Reduction. 11. Addition to Alkynes. 12. Chirality. 13. Substitution. 14. Elimination. 15. Radical Reactions. 16. Synthesis Workshop 1. 17. Conjugation and Molecular Orbital (MO) Theory. 18. Aromaticity. 19. EAS: Electrophilic Aromatic Substitution. 20. Acidity and pka of Phenols. 21. NAS: Nucleophilic Aromatic Substitution. 22. Synthesis Workshop 2. 23. Addition to a Carbonyl. 24. Carboxylic Acids & Derivatives. 25. Enolate & Enol Nucleophiles. 26. Aldol and Claisen Reactions. 27. Amines. Summary of Synthetic Transformations. Index. Table of pka Values by Structure. 2009, 528pp, Paperback, 9780618974122 ORGANIC CHEMISTRY, 2E With Biological Applications, International Edition John E. McMurry, Cornell University Renowned for its student-friendly writing style and fresh perspective, this fully updated Second Edition of John McMurry s ORGANIC CHEMISTRY: A BIOLOGICAL APPROACH, International Edition provides full coverage of the foundations of organic chemistry enhanced by biological examples throughout. Based on user feedback, McMurry continues to discuss the organic chemistry of biological pathways and now adds two dozen additional organic chemistry topics, as well as new problems, new illustrations, and new essays. Media integration with OWL for Organic Chemistry, a customizable online learning system and assessment tool, reduces faculty workload, facilitates instruction, and helps students master concepts through tutorials, simulations, and algorithmically generated homework questions. NEW TO THIS EDITION A NEW BOOK TITLE. The new title emphasizes that this Second Edition is a mainstream organic chemistry text written for the standard organic chemistry course taught in colleges and universities throughout the world. EARLIER COVERAGE OF STEREOCHEMISTRY AND SPECTROSCOPY. Based on user feedback, the chapter on chirality and stereochemistry at tetrahedral centers, a topic crucial to understanding biological chemistry, now appears much earlier in the book (Chapter 5), and the chapters on spectroscopy now precede the chapter on organohalides. ENHANCED PROBLEMS, EXAMPLES, ILLUSTRATIONS, & ESSAYS. To enhance problemsolving and visualization skills, McMurry increases 96

the number of multi-step problems and reduces the number of drill-type problems, increases the use of electrostatic potential maps that illustrate structure and reactivity, includes at least one MCAT worked example in every chapter, and includes new Green Chemistry essays. SIMPLIFIED COVERAGE. Based on user feedback, McMurry offers simplified coverage of amino acid metabolism, amino acid biosynthesis, nucleotide metabolism, and nucleotide biosynthesis. ADDITIONAL ORGANIC CHEMISTRY TOPICS: McMurry adds new coverage of: alkene ozonolysis and diol cleavage, carbenes to alkenes, the Diels Alder cycloaddition reaction, acetylide alkylations (8); aromatic ions, nucleophilic aromatic substitution, aromatic hydrogenation (9); allylic bromination of alkenes (12); Dess Martin oxidation of alcohols, protection of alcohols as silyl ethers, Claisen rearrangement (13); protection of ketones, aldehydes as acetals, conjugate addition of diorganocuprates to enones (14); Grignard reaction of nitriles (15); reduction of acid halides, Grignard reaction of acid halides, reaction of diorganocuprates with acid halides (16); and alpha bromination of carboxylic acids (17). VERTICAL FORMAT FOR CHEMICAL AND BIOCHEMICAL REACTION MECHANISMS. John McMurry s hallmark vertical format for mechanisms prints action steps vertically and explains changes taking place in each step next to the reaction arrows so students can see what is occurring at each step in a reaction without having to jump back and forth between the text and structures. VISUALIZATION OF BIOLOGICAL REACTIONS. McMurry ghosts the non-reacting parts of biological reactions to focus student attention on the reacting parts in large molecules, so they can more easily visualize changes that occur during reactions of large biomolecules. WHY THIS CHAPTER? INTRODUCTIONS. A brief paragraph in each chapter introduction tells students why the material about to be covered is important and explains how the organic chemistry in each chapter relates to biological chemistry. TITLES FOR EACH WORKED EXAMPLE. The worked examples in each chapter are titled to give students a frame of reference and each includes a strategy and worked-out solution, followed by problems for students to try on their own. LAGNIAPPES ( SOMETHING EXTRA ). McMurry s chapter-ending Lagniappes relate real-world concepts to students lives through essays. 1. Structure and Bonding. 2. Polar Covalent Bonds; Acids and Bases. 3. Organic Compounds: Alkanes and Their Stereochemistry. 4. Organic Compounds: Cycloalkanes and Their Stereochemistry. 5. Stereochemistry at Tetrahedral Centers. 6. An Overview of Organic Reactions. 7. Alkenes and Alkynes. 8. Reactions of Alkenes and Alkynes. 9. Aromatic Compounds. 10. Structure Determination: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy. 11. Structure Determination: Nuclear Magnetic Resonance Spectroscopy. 12. Organohalides: Nucleophilic Substitutions and Eliminations. 13. Alcohols, Phenols, and Thiols; Ethers and Sulfides. A PREVIEW OF CARBONYL CHEMISTRY. 14. Aldehydes and Ketones: Nucleophilic Addition Reactions. 15. Carboxylic Acids and Nitriles. 16. Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions. 17. Carbonyl Alpha-Substitution and Condensation Reactions. 18. Amines and Heterocycles. 19. Biomolecules: Amino Acids, Peptides, and Proteins. 20. Amino Acid Metabolism. 21. Biomolecules: Carbohydrates. 22. Carbohydrate Metabolism. 23. Biomolecules: Lipids and Their Metabolism. 24. Biomolecules: Nucleic Acids and Their Metabolism. 25. Secondary Metabolites: An Introduction to Natural Products Chemistry. 2011, 1152pp, Paperback, 9780495391470 97

ORGANIC CHEMISTRY, 13E A Short Course Harold Hart, Michigan State University; Christopher M. Hadad, Ohio State University; Leslie E. Craine, Central Connecticut State University; David J. Hart, The Ohio State University The only textbook designed specifically for the onesemester short course in organic chemistry, this market leader appeals to a range of non-chemistry science majors through its emphasis on practical, real-life applications, coverage of basic concepts, and engaging visual style. In contrast to other texts for the course that are streamlined versions of full-year texts, this text was created from the ground up to offer a writing style, approach, and selection of topics that uniquely meet the needs of the short course. The Thirteenth Edition builds on the strengths of previous editions through an updated, dynamic art program--online, on CD, and in the text--new content that keeps students current with developments in the organic chemistry field, and a revised lab manual. NEW TO THIS EDITION OWL INTEGRATION. Improve student learning outcomes with OWL, the #1 online homework and learning system for chemistry. Developed by chemistry instructors for teaching chemistry, OWL includes course management tools that make homework management a breeze, as well as advanced reporting and grade book features that save time in grading homework and tracking student progress. OWL enables you to address students different learning styles through tutorials, simulations, visualization exercises, and algorithmically-generated homework questions with answer-specific feedback. With OWL s mastery learning approach, students work at their own pace until they understand each concept/skill. OWL includes an ebook, enhanced with multimedia learning tools. UPDATED ART PROGRAM. The text s updated, visually dynamic art program is enhanced online, on CD, and in the text. NEW PROBLEMS AND SOLUTIONS. This edition offers over 1,000 clearly marked, new problems and solutions - an average of almost 60 per chapter to help students improve their problem-solving skills. Many of the new problems require students to develop their three-dimensional visualization skills. EXPANDED FOCUS ON GREEN CHEMISTRY. Updated and revised end-of-chapter exercises now include green chemistry. UPDATED A WORD ABOUT ESSAYS. These engaging essays--now assignable and accompanied by pedagogy -- motivate students by demonstrating how chemistry relates to other branches of science and to their everyday lives. Many of these essays examine emerging issues in green chemistry while others cover interesting topics such as Quinones and the Bombadier Beetle, Alkaloids and the Dart Poison Frog, Prostaglandins, and Aspirin and Pain. UPDATED A CLOSER LOOK AT BOXES. These updated boxes encourage students to develop their Web research skills by exploring topics ranging from mass spectrometry and carbon dating to Nobel laureates and protein chemistry to the polymerase chain reaction. Instructors may assign these activities, using them as a basis for class discussion or as a springboard for projects. VISUALLY DYNAMIC ART PROGRAM. The art program offers beautifully designed electrostatic potential maps to aid discussions of acid-base chemistry, as well as ball-and-stick structures that help students visualize molecules in three dimensions. USE OF ARROW PUSHING FORMALISM. This assists professors teaching reaction mechanisms. WORKED OUT EXAMPLES AND PRACTICE PROBLEMS. These exercises and problems guide students through learning and mastering chapter concepts. End-of-chapter problems gradually increase in difficulty, reinforcing basic principles and problemsolving skills before moving on to more challenging ones. ACCOMPANYING LABORATORY MANUAL. Developed with the assistance of co-author T.K. Vinod 98

at Western Illinois University, the lab manual includes an experiment on green chemistry, pre-laboratory exercises, and safety instructions to students. 1. Bonding and Isomerism. 2. Alkanes and Cyclalkanes; Conformational and Geometric Isomerism. 3. Alkenes and Alkynes. 4. Aromatic Compounds. 5. Stereoisomerism. 6. Organic Halogen Compounds; Substitution and Elimination Reactions. 7. Alcohols, Phenols, and Thiols. 8. Ethers and Epoxides. 9. Aldehydes and Ketones. 10. Carboxylic Acids and Their Derivatives. 11. Amines and Related Nitrogen Compounds. 12. Spectroscopy and Structure Determination. 13. Heterocyclic Compounds. 14. Synthetic Polymers. 15. Lipids and Detergents. 16. Carbohydrates. 17. Amino Acids, Peptides, and Proteins. 18. Nucleotides and Nucleic Acids. 2012, 608pp, Hardback, 9781111425562 ORGANIC CHEMISTRY, 13E A Brief Course, International Edition Harold Hart, Michigan State University; Christopher M. Hadad, Ohio State University; Leslie E. Craine, Central Connecticut State University; David J. Hart, The Ohio State University The only textbook designed specifically for the onesemester short course in organic chemistry, this market leader appeals to a range of non-chemistry science majors through its emphasis on practical, real-life applications, coverage of basic concepts, and engaging visual style. In contrast to other texts for the course that are streamlined versions of full-year texts, this text was created from the ground up to offer a writing style, approach, and selection of topics that uniquely meet the needs of the short course. The Thirteenth Edition builds on the strengths of previous editions through an updated, dynamic art program online, on CD, and in the text new content that keeps students current with developments in the organic chemistry field, and a revised lab manual. NEW TO THIS EDITION OWL INTEGRATION. Improve student learning outcomes with OWL, the #1 online homework and learning system for chemistry. Developed by chemistry instructors for teaching chemistry, OWL includes course management tools that make homework management a breeze, as well as advanced reporting and grade book features that save time in grading homework and tracking student progress. OWL enables you to address students different learning styles through tutorials, simulations, visualization exercises, and algorithmically-generated homework questions with answer-specific feedback. With OWL s mastery learning approach, students work at their own pace until they understand each concept/skill. OWL includes an ebook, enhanced with multimedia learning tools. UPDATED ART PROGRAM. The text s updated, visually dynamic art program is enhanced online, on CD, and in the text. UPDATED A WORD ABOUT ESSAYS. These engaging essays now assignable and accompanied by pedagogy motivate students by demonstrating how chemistry relates to other branches of science and to their everyday lives. Many of these essays examine emerging issues in green chemistry while others cover interesting topics such as Quinones and the Bombadier Beetle, Alkaloids and the Dart Poison Frog, Prostaglandins, and Aspirin and Pain. UPDATED A CLOSER LOOK AT BOXES. These updated boxes encourage students to develop their Web research skills by exploring topics ranging from mass spectrometry and carbon dating to Nobel laureates and protein chemistry to the polymerase chain reaction. Instructors may assign these activities, using them as a basis for class discussion or as a springboard for projects. VISUALLY DYNAMIC ART PROGRAM. The art program offers beautifully designed electrostatic potential maps to aid discussions of acid-base chemistry, as well as ball-and-stick structures that help students visualize molecules in three dimensions. 99

USE OF ARROW PUSHING FORMALISM. This assists professors teaching reaction mechanisms. WORKED OUT EXAMPLES AND PRACTICE PROBLEMS. These exercises and problems guide students through learning and mastering chapter concepts. End-of-chapter problems gradually increase in difficulty, reinforcing basic principles and problemsolving skills before moving on to more challenging ones. ACCOMPANYING LABORATORY MANUAL. Developed with the assistance of co-author T.K. Vinod at Western Illinois University, the lab manual includes an experiment on green chemistry, pre-laboratory exercises, and safety instructions to students. 1. Bonding and Isomerism. 2. Alkanes and Cyclalkanes; Conformational and Geometric Isomerism. 3. Alkenes and Alkynes. 4. Aromatic Compounds. 5. Stereoisomerism. 6. Organic Halogen Compounds; Substitution and Elimination Reactions. 7. Alcohols, Phenols, and Thiols. 8. Ethers and Epoxides. 9. Aldehydes and Ketones. 10. Carboxylic Acids and Their Derivatives. 11. Amines and Related Nitrogen Compounds. 12. Spectroscopy and Structure Determination. 13. Heterocyclic Compounds. 14. Synthetic Polymers. 15. Lipids and Detergents. 16. Carbohydrates. 17. Amino Acids, Peptides, and Proteins. 18. Nucleotides and Nucleic Acids. 2012, 608pp, Paperback, 9781111426248 ORGANIC CHEMISTRY Guided Inquiry for Recitation, Volume 2, International Edition Andrei Straumanis, College of Charleston Add the power of guided inquiry to your course without giving up lecture with ORGANIC CHEMISTRY: A GUIDED INQUIRY FOR RECITATION, Volume II, International Edition. Slim and affordable, the book covers key Organic 2 topics using POGIL (Process Oriented Guided Inquiry Learning), a proven teaching method that increases learning in organic chemistry. Containing everything you need to energize your teaching assistants and students during supplemental sessions, the workbook builds critical thinking skills and includes once-a-week, student-friendly activities that are designed for supplemental sessions, but can also be used in lab, for homework, or as the basis for a hybrid POGIL-lecture approach. EASILY ADAPTABLE TO ANY ORGANIC CHEMISTRY COURSE. This workbook makes it easy for you to take advantage of the benefits of Process Oriented Guided Inquiry Learning (POGIL) without giving up lecture. PERFECT FOR TEACHING ASSISTANTS OR UNDERGRADUATE PEER LEADERS. Designed to help you get more out of your TA or peer-led supplemental sessions, this workbook includes special To the TA sections that cover the nuts and bolts of a successful implementation. A WIDE RANGE OF FLEXIBLE ACTIVITIES. Choose from among the diverse set of C hemactivities that cover key Organic 2 topics and use them in whatever order works best for you. Each activity contains The Big Picture and Common Points of Confusion sections that steer students away from common pitfalls and toward an expert understanding of organic chemistry. PROVEN EFFECTIVE IN INCREASING STUDENT LEARNING. Students learn best when they are actively engaged and thinking in class and working to solve problems and understand concepts the way real scientists do, by analyzing data and asking questions. The workbook activities improve student understanding of lectures and textbook reading and help them do better on exams. Special To the Student sections cover the nuts and bolts of using the workbook effectively. 1. Aromaticity. 2. Introduction to EAS. 3. EAS Resonance Effects. 4. EAS Competing Effects. 5. EAS Synthesis Workshop. 6. Grignard and Lithium Reagents. 7. Nucleophilic Addition-Elimination. 8. Carboxylic Acids 100

and Derivatives. 9. Acid Halides and Anhydrides. 10. Enol and Enolate Nucleophiles. 11. Aldol Reactions. 12. Aldol Condensations. 13. Claisen & Michael Reactions. 14. Amines. 15. Carbon (13C) NMR. 16. Proton (1H) NMR. Appendix. NW3: Naming Aromatic Compounds. NW4: Naming Carbonyl Compounds. 2012, 224pp, Paperback, 9781111578305 ORGANIC CHEMISTRY A Guided Inquiry for Recitation, Volume 1, International Edition Andrei Straumanis, College of Charleston Add the power of guided inquiry to your course without giving up lecture with ORGANIC CHEMISTRY: A GUIDED INQUIRY FOR RECITATION, Volume I, International Edition. Slim and affordable, the book covers key Organic 1 topics using POGIL (Process Oriented Guided Inquiry Learning), a proven teaching method that increases learning in organic chemistry. Containing everything you need to energize your teaching assistants and students during supplemental sessions, the workbook includes once-a-week, studentfriendly activities that are designed for supplemental sessions, but can also be used in lab, for homework, or as the basis for a hybrid POGIL-lecture approach. EASILY ADAPTABLE TO ANY ORGANIC CHEMISTRY COURSE. This workbook makes it easy for you to take advantage of the benefits of Process Oriented Guided Inquiry Learning (POGIL) without giving up lecture. PERFECT FOR TEACHING ASSISTANTS OR UNDERGRADUATE PEER LEADERS. Designed to help you get more out of your TA or peer-led supplemental sessions, this workbook includes special To the TA sections that cover the nuts and bolts of a successful implementation. A WIDE RANGE OF FLEXIBLE ACTIVITIES. Choose from among 18 ChemActivities covering key Organic 1 topics and use them in whatever order works best for you. Each activity contains The Big Picture and Common Points of Confusion sections that steer students away from common pitfalls and toward an expert understanding of organic chemistry. PROVEN EFFECTIVE IN INCREASING STUDENT LEARNING. Students learn best when they are actively engaged and thinking in class and working to solve problems and understand concepts the way real scientists do, by analyzing data and asking questions. The workbook activities improve student understanding of lectures and textbook reading and help them do better on exams. Special To the Student sections cover the nuts and bolts of using the workbook effectively. 1. Lewis Structures. 2. Resonance. 3. Constitutional Isomers. 4. Cycloalkane Stereoisomers. 5. Alkene Stereoisomers. 6. Addition to Alkenes. 7. Radical Halogenation. 8. Chiral Centers. 9. Absolute Configuration (R/S). 10. One-Step Nucleophilic Substitution (SN2). 11. Two-Step Nucleophilic Substitution (SN1). 12. Two- Step Elimination (E1). 13. One-Step Elimination (E2). 14. Sorting out E1, E2, SN1, SN2. 15. Retrosynthesis. 16. Carbon (13C) NMR. 17. Proton (1H) NMR. Appendix. NW1-Nomenclature of Alkanes. NW2-Introduction to Naming Functional Groups. 2012, 224pp, Paperback, 9781111578299 ORGANIC CHEMISTRY WITH BIOLOGICAL APPLICATIONS, 3E John E. McMurry, Cornell University 101

Renowned for its student-friendly writing style and fresh perspective, this fully updated Third Edition of John McMurry s ORGANIC CHEMISTRY WITH BIOLOGICAL APPLICATIONS provides full coverage of the foundations of organic chemistry--enhanced by biological examples throughout. In addition, McMurry discusses the organic chemistry behind biological pathways. New problems, illustrations, and essays have been added. Media integration with OWL for Organic Chemistry, a customizable online learning system, and assessment tool, reduces faculty workload, facilitates instruction, and helps students master concepts through tutorials, simulations, and algorithmicallygenerated homework questions. NEW TO THIS EDITION WHY THIS CHAPTER? now begins each chapter; it is a brief introduction about the material being covered, why it is important and how the organic chemistry in the chapter relates to biological chemistry. Figure and table references in the text are now in color to help reference them. All figure legends now begin with a boldface title to help students easily identify their content. SOMETHING EXTRA essays end each chapter and tie the chapter content to relevant real-world material. Some new essays include, Organic Foods, and Dental Anesthetics. Many new problems have been included at the end of chapters. Some new content includes: Mercury-catalyzed alkyne hydration (Chapter 8); Enols and tautomerization (Chapter 8); Conversion of alcohols to alkyl fluorides (Chapter 12); Organic coupling reactions (Chapter 12); Base-induced epoxide cleavage (Chapter 13); Killiani-Fischer and Whol degradation (Chapter 21); Prostaglandins and other eicosanoids (Chapter 23). An increase in the number of Organic OWL questions for the online homework system. The #1 online homework and learning system for chemistry, OWLv2, is available for this text--now with new instructor features and enhanced functionality: a Dashboard that consolidates all course materials; easy, intuitive assignment creation and management; ability to preview and select activities/questions for each assignment; new assignment settings and options; improved gradebook; Personalized Study tools to help students focus their time on the key concepts and skills; and MindTap Reader, a new ebook with apps and embedded video. OWLv2 courses for Gen Chem, GOB, Organic, and Liberal Arts now include Quick Prep essential skills assignments that can be taken before the semester begins or during the first few weeks, to help students succeed in the course. For this course, OWLv2 also includes new interactive versions of the end-of-chapter questions from the text and new ipad-compatible visualizations and tutorials. EARLIER COVERAGE OF STEREOCHEMISTRY AND SPECTROSCOPY. Chirality and stereochemistry at tetrahedral centers, a topic crucial to understanding biological chemistry, appears early in Chapter 5. ENHANCED PROBLEMS. To enhance problem-solving and visualization skills, McMurry uses many multistep problems and reduces the number of drill-type problems. VERTICAL FORMAT FOR CHEMICAL AND BIOCHEMICAL REACTION MECHANISMS. Mechanisms are printed with action steps vertically, alongside annotations for each step next, so students can see what is occurring at each step in a reaction without having to jump back and forth between the text and structures. 1. Structure and Bonding. 2. Polar Covalent Bonds; Acids and Bases. 3. Organic Compounds: Alkanes and Their Stereochemistry. 4. Organic Compounds: Cycloalkanes and Their Stereochemistry. 5. Stereochemistry at Tetrahedral Centers. 6. An Overview of Organic Reactions. 7. Alkenes and Alkynes. 8. Reactions of Alkenes and Alkynes. 9. Aromatic Compounds. 10. Structure Determination: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy. 11. Structure Determination: Nuclear Magnetic Resonance Spectroscopy. 12. Organohalides: Nucleophilic Substitutions and Eliminations. 13. Alcohols, Phenols, and Thiols; Ethers and Sulfides: A Preview of Carbonyl Chemistry 14. Aldehydes and Ketones: Nucleophilic Addition Reactions. 15. Carboxylic Acids and Nitriles. 16. Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions. 17. Carbonyl Alpha-Substitution and Condensation Reactions. 18. Amines and Heterocycles. 19. Biomolecules: 102

Amino Acids, Peptides, and Proteins. 20. Amino Acid Metabolism. 21. Biomolecules: Carbohydrates. 22. Carbohydrate Metabolism. 23. Biomolecules: Lipids and Their Metabolism. 24. Biomolecules: Nucleic Acids and Their Metabolism. e25. Secondary Metabolites: An Introduction to Natural Products Chemistry. e26. Orbitals and Organic Chemistry: Pericyclic Reactions. e27. Synthetic Polymers. 2015, 1128pp, Hardback, 9781285842912 ORGANIC CHEMISTRY, INTERNATIONAL EDITION, 7E William H. Brown, Beloit College; Brent L. Iverson, University of Texas, Austin; Eric Anslyn, University of Texas at Austin; Christopher S. Foote, University of California, Los Angeles Providing a modern introduction to organic chemistry for students majoring in chemistry, health, and the biological sciences, this revised and updated edition of ORGANIC CHEMISTRY, 7E, International Edition is both student-friendly and cutting-edge and incorporates the latest advances in the field. Professors Brown, Iverson, and Anslyn have all won teaching awards at their respective schools, and they use their skills to build upon the text s hallmarks of unified mechanistic themes, focused problem-solving, use of applied problems from the pharmaceutical field, and unrivaled visuals. Thoroughly updated throughout, the book offers numerous biological examples for pre-med students, a wide range of in-text learning tools, and integration with both a homework and tutorial system and an interactive multimedia ebook. To help students understand reaction mechanisms, the authors offset them in a stepwise fashion and emphasize similarities between related mechanisms using just four different characteristics: breaking a bond, making a new bond, adding a proton and taking a proton away. Organic chemistry reaction roadmaps take a center stage in this edition with new pull-out maps designed in a stepwise manner by chapter. These roadmaps will help students to devise their own reaction pathways. Numerous resources help ensure student success in the course, including a running margin glossary, a mini end-of-chapter in-text study guide, and more inchapter examples than any other text on the market. Emphasizing how-to skills, this edition is packed with challenging synthesis problems, medicinal chemistry problems, and unique roadmap problems. NEW TO THIS EDITION MCAT PROBLEMS: To better prepare students for the upcoming new MCAT exam, the new edition includes MCAT PRACTICE: PASSAGE AND PROBLEMS throughout the text. First students read the organic chemistry-related essay and then answer a series of multiple-choice questions. NEW PRIMERS: Two new primers (Developing a Reaction Mechanism before Chapter 6 and Carboxylic Acid Derivative Reaction Mechanisms before Chapter 18) set key and possibly difficult concepts apart for easy reference to enhance student understanding. NEWLY-DRAWN ORGANIC CHEMISTRY REACTION ROADMAPS: Creating a cumulative, graphical representation of the different reactions students encounter in the context of important functional groups, the organic chemistry roadmaps help students visualize how to interconvert different functional groups (which often require different reactions from different chapters) by simply identifying the most direct path on the roadmap. New pull out cards show the roadmaps in sequential order. REVISED REACTION ROADMAP PROBLEMS: These unique problems relate to the authors organic chemistry roadmap (see above), which compares organic chemistry to a roadmap, with functional groups analogous to cities and reactions analogous to the roads between them. FIVE NEW HOW TO BOXES: Integrated throughout the text at strategic points, the new boxes show students: How To: Quickly Figure Out Formal Charge, How To: Quickly Recognize the Hybridization and Geometry of Atoms, How To: Quickly Draw and Recognize Enantiomers and Diastereomers, How To: Retrosynthetically Dissect an Amine into the Proper Starting Materials for a Reductive Amination, and 103

How To: Recognize Aromatic Compounds: Criteria and Caveats. PRESENTATION OF MECHANISMS: Mechanisms are presented in a clear, stepwise fashion with written commentary accompanying each mechanistic step so verbal learners can learn alongside more visually oriented learners. Many mechanisms have been broken into more steps to increase student understanding. In addition, the authors emphasize similarities between related mechanisms using just four different characteristics: breaking a bond, making a new bond, adding a proton, and taking a proton away. A new primer (right before Chapter 6) on Developing a Reaction Mechanism sets this material apart for easy reference. VISUAL IMPACT: This text is distinguished by its striking, full-color art program (250 pieces of numbered art and over 1,000 pieces of in-text art). The Seventh Edition paints a detailed picture of the orbital nature of electron density in Chapter 1 by focusing on the interplay between the two complementary approaches to orbital descriptions: valence bond theory and molecular orbital theory. High-quality photos show organic chemistry as it occurs in the laboratory and in everyday life; electrostatic potential maps illustrate structure and reactivity; the spectra in the book reflects the latest imagery; and the book includes state-of-the-art, mathematically accurate molecular models. HOW-TO BOXES: To facilitate student success in the course, insightful How-To boxes highlight the survival skills necessary to learn and master organic chemistry. Integrated throughout the text at key points, these essential skills include How To: Draw Curved Arrows and Push Electrons, How To: Draw Chiral Molecules, How To: Solve NMR Spectral Problems, and many more. Five new How To boxes to this edition are, How To: Quickly Figure Out Formal Charge, How To: Quickly Recognize the Hybridization and Geometry of Atoms, How To: Quickly Draw and Recognize Enantiomers and Diastereomers, How To: Retrosynthetically Dissect an Amine into the Proper Starting Materials for a Reductive Amination, and How To: Recognize Aromatic Compounds: Criteria and Caveats. BIOLOGY CONNECTION: Although still a predominantly synthetic organic chemistry text, the book explicitly links concepts to biological chemistry topics--drawing in biology majors, pre-med students, and others who will soon go on to biochemistry. Connections to Biological Chemistry boxes discuss the applications of organic chemistry to biology to a wide range of topics. REACTIONS IN CONTEXT: These problems apply organic chemistry to medicinal chemistry and the pharmaceutical sciences. 1. Covalent Bonding and Shapes of Molecules. 2. Alkanes and Cycloalkanes. 3. Stereochemistry and Chirality. 4. Acids and Bases. 5. Alkenes. Primer I: Reaction Mechanisms 6. Reactions of Alkenes. 7. Alkynes. 8. Haloalkanes, Halogenation, and Radical Reactions. 9. Nucleophilic Substitution and B-Elimination. 10. Alcohols. 11. Ethers, Sulfides, and Epoxides. 12. Infrared Spectroscopy. 13. Nuclear Magnetic Resonance Spectroscopy. 14. Mass Spectrometry. 15. Introduction to Organometallic Compounds. 16. Aldehydes and Ketones. 17. Carboxylic Acids. Primer II: Carboxylic Acid Derivative Reaction Mechanisms. 18. Functional Derivatives of Carboxylic Acids. 19. Enolate Anions and Enamines. 20. Dienes, Conjugated Systems, and Pericyclic Reactions. 21. Benzene and the Concept of Aromaticity. 22. Reactions of Benzene and Its Derivatives. 23. Amines. 24. Catalytic Carbon Carbon Bond Formation. 25. Carbohydrates. 26: Lipids. 27. Amino Acids and Proteins. 28. Nucleic Acids. 29. Organic Polymer Chemistry. Appendices: 1. Thermodynamics and the Equilibrium Constant. 2. Major Classes of Organic Acids. 3. Bond Dissociation Enthalpies. 4. Characteristic 1H-NMR Chemical Shifts. 5. Characteristic 13C Chemical Shifts. 6. Characteristic IR Absorption Frequencies. 7. Electrostatic Potential Maps. 8. Summary of Stereochemical Terms. 9. Summary of the Rules of Nomenclature. 10. Common Mistakes in Arrow Pushing. 11. Organic Chemistry Roadmaps. GLOSSARY G-1. INDEX I-1. 2014, 1312pp, Paperback, 9781285052816 104

ORGANIC CHEMISTRY, INTERNATIONAL EDITION, 8E John E. McMurry, Cornell University The most trusted and best-selling text for organic chemistry just got better! Updated with the latest developments, expanded with more end-of-chapter problems, reorganized to cover stereochemistry earlier, and enhanced with OWL, the leading online homework and learning system for chemistry, John McMurry s ORGANIC CHEMISTRY, 8e, International Edition continues to set the standard for the course. The Eighth Edition also retains McMurry s hallmark qualities: comprehensive, authoritative, and clear. McMurry has developed a reputation for crafting precise and accessible texts that speak to the needs of instructors and students. More than a million students worldwide from a full range of universities have mastered organic chemistry through his trademark style, while instructors at hundreds of colleges and universities have praised his approach time and time again. NEW TO THIS EDITION IMPROVED CHAPTER-ENDING PROBLEM ORGANIZATION. End-of-chapter problems are now grouped by type to assist professors in assigning problems and students in solving them. EARLIER COVERAGE OF STEREOCHEMISTRY. Stereochemistry now appears earlier in the book (Chapter 5) to get to this important topic sooner in the course. In addition, Cahn Ingold Prelog sequence rules are now introduced in Section 5.5. REVISISED COVERAGE OF FUNDAMENTAL TOPICS. The revision of activation energies in multistep reactions and the update of all bond dissociation energies in Chapter 6 helps students to better understand this fundamental topic. REVISED END-OF-CHAPTER QUESTIONS IN OWL. The integrated OWL online learning system now includes more parameterized end-of-chapter questions, encouraging students to practice multiple questions of the same type with different chemicals, wording, and numbers to ensure their mastery of the underlying chemical concepts. OWL also includes an interactive e-version of the textbook, enhanced with rich multimedia learning tools and available 24/7 in OWL. REVISED FOCUS ON BOXES. These end-of-chapter boxes now present interesting applications of organic chemistry relevant to the particular chapter. UPDATED FIGURES. To better coordinate legends with art, step numbers have been added to the legends of all mechanism figures. In addition, all figure references have been more clearly keyed to illustrations via color. NEW SUPPLEMENT. SPARTAN MODEL: AN ELECTRONIC MODEL KIT is now available to package with the Eighth Edition for those who want to use this advanced technology resource. VERTICAL FORMAT FOR REACTION MECHANISMS. McMurry s hallmark vertical format is used to explain reaction mechanisms. The mechanisms are printed vertically while explanations of the changes taking place in each step are printed next to the reaction arrow. This allows students to easily see what is occurring at each step in a reaction without having to jump back and forth between the text and structures. UNIQUE COVERAGE. McMurry emphasizes organic synthesis as a teaching device to help students organize and work with the large body of factual information that makes up organic chemistry. He also offers an unusually complete treatment of the organic chemistry of nucleic acids and an integrated treatment of polymer chemistry. PROBLEM-SOLVING FOCUS. Each chapter contains many worked out examples with Strategy Statements that illustrate how to solve problems. Each practice problem and solution is then followed by a similar problem for the student to solve. This provides immediate problem-solving reinforcement for the student. 1. Structure and Bonding. 2. Polar Covalent Bonds; Acids and Bases. 3. Organic Compounds: Alkanes and Their 105

Stereochemistry. 4. Organic Compounds: Cycloalkanes and Their Stereochemistry. 5. Stereochemistry at Tetrahedral Centers. 6. An Overview of Organic Reactions. 7. Alkenes: Structure and Reactivity. 8. Alkenes: Reactions and Synthesis. 9. Alkynes: An Introduction to Organic Synthesis. 10. Organohalides. 11. Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations. 12. Structure Determination: Mass Spectrometry and Infrared Spectroscopy. 13. Structure Determination: Nuclear Magnetic Resonance Spectroscopy. 14. Conjugated Compounds and Ultraviolet Spectroscopy. 15. Benzene and Aromaticity. 16. Chemistry of Benzene: Electrophilic Aromatic Substitution. 17. Alcohols and Phenols. 18. Ethers and Epoxides; Thiols and Sulfides. Preview of Carbonyl Chemistry. 19. Aldehydes and Ketones: Nucleophilic Addition Reactions. 20. Carboxylic Acids and Nitriles. 21. Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions. 22. Carbonyl Alpha-Substitution Reactions. 23. Carbonyl Condensation Reactions. 24. Amines and Heterocycles. 25. Biomolecules: Carbohydrates. 26. Biomolecules: Amino Acids, Peptides, and Proteins. 27. Biomolecules: Lipids. 28. Biomolecules: Nucleic Acids. 29. The Organic Chemistry of Metabolic Pathways. 30. Orbitals and Organic Chemistry: Pericyclic Reactions. 31. Synthetic Polymers. 2012, 1376pp, Paperback, 9780840054531 ORGANIC EXPERIMENTS, 6E Macroscale and Microscale, International Edition Kenneth L. Williamson, Mount Holyoke College, Emeritus; Katherine M. Masters, Pennsylvania State University The market leader for the full-year organic laboratory, this manual derives many experiments and procedures from the classic Feiser lab text, giving it an unsurpassed reputation for solid, authoritative content. The Sixth Edition includes new experiments that stress greener chemistry, as well as updated NMR spectra and a Premium Website that includes glassware-specific videos with pre-lab, gradable exercises. Offering a flexible mix of macroscale and microscale options for most experiments, this proven manual emphasizes safety and allows instructors to save on the purchase and disposal of expensive, sometimes hazardous, organic chemicals. Macroscale versions can be used for less costly experiments, allowing students to get experience working with conventionally-sized glassware. NEW TO THIS EDITION UPDATED NMR SPECTRA. The authors have fully updated NMR spectra throughout the manual. NEW AND UPDATED LABS AND EXPERIMENTS. Many labs have been updated, and new lab experiments include A Diels-Alder Reaction Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride and Multicomponent Reactions: The Aqueous Passerini Reaction, and Virstatin, a Possible Treatment for Cholera. PREMIUM WEBSITE. A new Premium Website includes glassware-specific videos with pre-lab, gradable exercises. GREENER CHEMISTRY. Experiments that stress greener chemistry appear throughout the manual and are identified with a green chemistry icon. For example, the use of household bleach is explored as an alternative to the toxic chromium ion as an oxidizing agent for cyclohexanol. AN EMPHASIS ON LABORATORY SAFETY. The laboratory safety chapter includes material on working with closed systems and laboratory courtesy. A STRONG MASS SPECTROMETRY CHAPTER. The chapter on mass spectrometry describes time-offlight and mass quadrupole analyzers and includes sections on GC-MS and computer-aided spectral identification, as well as ESI and MALDI ionization. BIOASSAY EXPERIMENTS. The manual s bioassay experiments include a bioassay of eugenol isolated from cloves. COMPREHENSIVE COVERAGE. Material is offered on diffuse reflectance IR analysis, capillary GC, and temperature programming. 106

1. Introduction. 2. Laboratory Safety, Courtesy, and Waste Disposal. 3. Melting Points and Boiling Points. 4. Recrystallization. 5. Distillation. 6. Steam Distillation, Vacuum Distillation, and Sublimation. 7. Extraction. 8. Thin-Layer Chromatography: Analyzing Analgesics and Isolating Lycopene from Tomato Paste. 9. Column Chromatography: Fluorenone, Cholesteryl Acetate, Acetylferrocene, and Plant Pigments. 10. Gas Chromatography: Analyzing Alkene Isomers. 11. Infrared Spectroscopy. 12. Nuclear Magnetic Resonance Spectroscopy. 13. Mass Spectrometry. 14. Ultraviolet Spectroscopy, Refractive Indices, and Qualitative Instrumental Organic Analysis. 15. Computational Chemistry. 16. The SN2 Reaction: 1-Bromobutane. 17. Nucleophilic Substitution Reactions of Alkyl Halides. 18. Radical Initiated Chlorination of 1-Chlorobutane. 19. Alkenes from Alcohols: Cyclohexene from Cyclohexanol. 20. Bromination and Debromination: Purification of Cholesterol. 21. Dichlorocarbene. 22. Oxidation: Cyclohexanol to Cyclohexanone; Cyclohexanone to Adipic Acid. 23. The Cannizzaro Reaction: Simultaneous Synthesis of an Alcohol and an Acid in the Absence of Solvent. 24. Oxidative Coupling of Alkynes: 2,7-Dimethyl-3,5-octadiyn-2,7-diol. 25. Catalytic Hydrogenation. 26. Sodium Borohydride Reduction of 2-Methylcyclohexanone: A Problem in Conformational Analysis. 27. Epoxidation of Cholesterol. 28. Nitration of Methyl Benzoate. 29. Friedel-Crafts Alkylation of Benzene and Dimethoxybenzene; Host-Guest Chemistry. 30. Alkylation of Mesitylene. 31. The Friedel-Crafts Reaction: Anthraquinone and Anthracene. 32. Friedel-Crafts Acylation of Ferrocene: Acetylferrocene. 33. Reactions of Triphenylmethyl Carbocation, Carbanion, and Radical. 34. 1,2,3,4-Tetraphenylnaphthalene via Benzyne. 35. Triptycene via Benzyne. 36. Aldehydes and Ketones. 37. Dibenzalacetone by the Aldol Condensation. 38. Grignard Synthesis of Triphenylmethanol and Benzoic Acid. 39. The Wittig and Wittig-Horner Reactions. 40. Esterification and Hydrolysis. 41. Acetylsalicylic Acid (Aspirin). 42. Malonic Ester of a Barbiturate. 43. Amines. 44. The Sandmeyer Reaction: 1-Bromo-4-chlorobenzene, 2-Iodobenzoic Acid, and 4-Chlorotoluene. 45. Synthesis and Bioassay of Sulfanilamide and Derivatives. 46. Dyes and Dyeing. 47. Martius Yellow. 48. Diels-Alder Reaction. 49. Ferrocene [Bis(cyclopentadienyl)iron]. 50. A Diels-Alder Reaction Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride. 51. Tetraphenylcyclopentadienone. 52. Hexaphenylbenzene and Dimethyl Tetraphenylphthalate. 53. The Benzoin Condensation: Catalysis by the Cyanide Ion and Thiamine. 54. Nitric Acid Oxidation; Preparation of Benzil from Benzoin; and Synthesis of a.heterocycle: Diphenylquinoxaline. 55. The Borohydride Reduction of a Ketone: Hydrobenzoin from Benzil. 56. The Synthesis of 2,2-Dimethyl-1,5-dioxolane; The Acetonide Derivative of a Vicinal Diol. 57. 1,4-Addition: Reductive Acetylation of Benzil. 58. The Synthesis of an Alkyne from an Alkene; Bromination and Dehydrobromination: Stilbene and Diphenylacetylene. 59. The Perkin Reaction: Synthesis of α-phenylcinnamic Acid and Its Decarboxylation to cis- Stilbene. 60. Multicomponent Reactions: The Aqueous Passerini Reaction. 61. Chemiluminescence: Syntheses of Cyalume and Luminol. 62. Photochemistry: The Synthesis of Benzopinacol. 63. Carbohydrates and Sweeteners. 64. Virstatin, a Possible Treatment for Cholera. 65. Biosynthesis of Ethanol and Enzymatic Reactions. 66. The Synthesis of Natural Products: Pseudopellitierene and Camphor. 67. Polymers: Synthesis and Recycling. 68. Searching the Chemical Literature. 2011, 880pp, Paperback, 9780538733632 PUSHING ELECTRONS, 4E Daniel P. Weeks, Northwestern University This brief supplemental guidebook assists students in mastering the difficult concept of pushing electrons that is essential to success in Organic Chemistry. With an investment of only 12 to 16 hours of self-study your students will have a better understanding of how to write resonance structures and will become comfortable with bond-making and bond-breaking steps in organic mechanisms. The low-tech, paper-onpencil approach uses active involvement and repetition 107

to teach students to properly push electrons to generate resonance structures and write organic mechanisms with a minimum of memorization. Compatible with any organic chemistry textbook. NEW TO THIS EDITION All structures redrawn with attention to correcting all bond lengths and angles. Updated and enhanced figures throughout the book. A new chapter added on the mechanisms for making synthetic polymers. A new section added on constitutional isomers. A new section added on correcting common mechanistic mistakes. Textual revisions to clarify some sections. The key to the success of this book is that it knows its place. It is a supplement that should be assigned alongside a textbook, not as a textbook replacement or a standalone product. The best way to market this book would be to convince ochem instructors that this will be a terrific 8-10 hr supplement that will be a great investment for getting their students up to speed with mechanisms. This step-by-step mechanistic approach fills an important hole that textbooks don t cover. Helps students master to critical concept of pushing electrons. Entire program requires only 12 to 16 hours of students time through self-study. A paper-on-pencil approach uses active involvement and repetition to teach the student. 1. Lewis Structures. 2. Resonance Structures. 3. Mechanisms. 4. On Solving Mechanism Problems. 5. Some Reactiosn from Biochemistry. STUDY GUIDE WITH SOLUTIONS MANUAL FOR BROWN/IVERSON/ ANSLYN/FOOTE S ORGANIC CHEMISTRY, 7E William H. Brown, Beloit College; Brent L. Iverson, University of Texas, Austin; Eric Anslyn, University of Texas at Austin; Christopher S. Foote, University of California, Los Angeles The perfect way to prepare for exams, build problemsolving skills, and get the grade you want! Offering detailed solutions to all in-text and end-of-chapter problems, this comprehensive guide helps you achieve a deeper intuitive understanding of chapter material through constant reinforcement and practice. The result is much better preparation for in-class quizzes and tests, as well as for national standardized tests such as the DAT and MCAT. 2014, 848pp, Paperback, 9781285052618 2014, 224pp, Paperback, 9781133951889 STUDY GUIDE WITH SOLUTIONS MANUAL FOR MCMURRY S ORGANIC CHEMISTRY: WITH BIOLOGICAL APPLICATIONS, 3E John E. McMurry, Cornell University This Study Guide and Solutions Manual provide answers and explanations to all in-text and end-of-chapter 108

exercises and include supplemental information to help enrich your chemistry experience. 2015, 704pp, Paperback, 9781305087972 STUDY GUIDE WITH STUDENT SOLUTIONS MANUAL FOR MCMURRY S ORGANIC CHEMISTRY, 8E John E. McMurry, Cornell University Written by Susan McMurry, the Study Guide and Solutions Manual provide answers and explanations to all in-text and end-of-chapter exercises. Content has been updated to match the new in-text and endof-chapter exercises. 2012, 912pp, Paperback, 9780840054456 TECHNIQUES LABS FOR MACROSCALE AND MICROSCALE ORGANIC EXPERIMENTS (WITH COURSEMATE 2-SEMESTER PRINTED ACCESS CARD), 6E Kenneth L. Williamson, Mount Holyoke College, Emeritus; Katherine M. Masters, Pennsylvania State University Succeed in your organic laboratory course with TECHNIQUES LABS FOR MACROSCALE AND MICROSCALE ORGANIC EXPERIMENTS, Sixth Edition. This proven, authoritative manual emphasizes safety and features new experiments that stress greener chemistry, as well as updated NMR spectra and a Premium Website that includes glasswarespecific videos with pre-lab, gradable exercises. Using the manual s mix of macroscale and microscale experiments, you ll gain the knowledge and confidence you need to perform a wide variety of experiments, as well as experience working with conventionally-sized glassware. NEW TO THIS EDITION UPDATED NMR SPECTRA. The authors have fully updated NMR spectra throughout the manual. NEW AND UPDATED LABS AND EXPERIMENTS. Many labs have been updated, and new lab experiments include A Diels-Alder Reaction Puzzle: The Reaction of 2,4-Hexadien-1-ol with Maleic Anhydride and Multicomponent Reactions: The Aqueous Passerini Reaction, and Virstatin, a Possible Treatment for Cholera. NEW FOCUS ON GREEN CHEMISTRY. In addition to providing 10 new experiments that stress green chemistry, the authors offer tips on how to think green when doing the labs. PREMIUM WEBSITE. A new Premium Website includes glassware-specific videos with pre-lab, gradable exercises. ADDITIONAL EXPERIMENTS ON THE COMPANION WEBSITE. Experiments from the author s best-selling MACROSCALE AND MICROSCALE ORGANIC EXPERIMENTS not included in this print manual are all available for download on the companion website GREENER CHEMISTRY. Experiments that stress greener chemistry appear throughout the manual and are identified with a green chemistry icon. For example, the use of household bleach is explored as an alternative to the toxic chromium ion as an oxidizing agent for cyclohexanol. AN EMPHASIS ON LABORATORY SAFETY. The laboratory safety chapter includes material on working with closed systems and laboratory courtesy. A STRONG MASS SPECTROMETRY CHAPTER. The chapter on mass spectrometry describes time-offlight and mass quadrupole analyzers and includes 109

sections on GC-MS and computer-aided spectral identification, as well as ESI and MALDI ionization. BIOASSAY EXPERIMENTS. The manual s bioassay experiments include a bioassay of eugenol isolated from cloves. COMPREHENSIVE COVERAGE. Material is offered on diffuse reflectance IR analysis, capillary GC, and temperature programming. 1. Introduction. 2. Laboratory Safety, Courtesy, and Waste Disposal. 3. Melting Points and Boiling Points. 4. Recrystallization. 5. Distillation. 6. Steam Distillation, Vacuum Distillation, and Sublimation. 7. Extraction. 8. Thin-Layer Chromatography: Analysis of Analgesics and Isolating Lycopene from Tomato Paste. 9. Column Chromatography: Fluorenone, Cholesteryl Acetate, Acetylferrocene, and Plant Pigments. 10. Gas Chromatography: Analysis of Alkene Isomers. 11. Infrared Spectroscopy. 12. Nuclear Magnetic Resonance Spectroscopy. 13. Mass Spectroscopy. 14. Ultraviolet Spectroscopy, Refractive Indices, and Qualitative Instrumental Organic Analysis. 15. Computational Chemistry. 2012, 336pp, Paperback, 9781111430412 UNDERSTANDING THE PRINCIPLES OF ORGANIC CHEMISTRY A Laboratory Course, Reprint, International Edition Steven F. Pedersen, University of California - Berkeley; Arlyn M. Myers, University of California - Berkeley Class-tested by thousands of students and using simple equipment and green chemistry ideas, UNDERSTANDING THE PRINCIPLES OF ORGANIC CHEMISTRY: A LABORATORY COURSE, International Edition includes 37 experiments that introduce traditional, as well as recently developed synthetic methods. Offering up-to-date and novel experiments not found in other lab manuals, this innovative book focuses on safety, gives students practice in the basic techniques used in the organic lab, and includes microscale experiments, many drawn from the recent literature. An Online Instructor s Manual available on the book s instructor s companion website includes helpful information, including instructors notes, pre-lab meeting notes, experiment completion times, answers to end-of-experiment questions, video clips of techniques, and more. SAFETY NOTES in each experiment warn students about potential hazards, CHEMICAL SAFETY NOTES emphasize the proper handling of reagents, and TECHNIQUE TIPS give students guidelines for handling equipment and using proper procedures. REFERENCES TO TOPICS IN UNDERGRADUATE TEXTBOOKS and/or the primary literature in the experiments reinforce the importance of what students are learning in the lecture course and demonstrate how text material relates to the laboratory. INTRODUCTORY ESSAYS in the experiments expose students to the history and practical applications of laboratory science. Within many experiments, DID YOU KNOW? boxes provide a brief, interesting fact about one of the chemicals used in the experiment. A CONSISTENT FORMAT for each experiment includes Background Reading, Prelab Checklist, Experimental Procedure, and Cleanup. Instructors may choose to offer the optional PREMIUM ORGANIC CHEMISTRY LABORATORY TECHNIQUES WEBSITE, which contains 33 videos on basic organic laboratory techniques. Each video has a series of questions with instant grading and feedback, so students can test their understanding of the concepts and email their assessment results to their instructors. PART I: THE THEORY AND TECHNIQUES. 1. Safety in the Chemistry Lab. 2. The Laboratory Notebook and the Laboratory Period. 3. Where to Find It: Searching the Literature. 4. Things You Need to Know Before You Begin. 5. Properties of Organic Molecules. 6. Characteristic Physical Properties of Pure Compounds. 110

7. Isolation and Purification of Compounds. 8. Structure Determination. 9. Running a Synthetic Reaction. PART II: THE EXPERIMENTS. Experiment 1. Calibrating a Pasteur Pipette. Experiment 2. Investigating Solubility and Acid-Base Reactions. Experiment 3. Mixed Melting Points. Experiment 4. Whittling Down the Possibilities: Identifying an Unknown Using Molecular Dipole Moment, Solubility, Density and Boiling Point Data. Experiment 5. Recrystallization and Melting Points: Recrystallization of Adipic and Salicylic Acids. Experiment 6. Recrystallization and Melting Points: Recrystallization of an Unknown Solid and the Decolorization of Brown Sugar. Experiment 7. Thin Layer Chromatography (TLC). Experiment 8. Identification of an Adulterated Herb or Spice by Thin Layer Chromatography (TLC). Experiment 9. What Do You Take for Pain? Experiment 10. Nucleophilic Substitution Reactions of Alkyl Halides. Experiment 11. The Isolation of Trimyristin from Nutmeg. Experiment 12. The Magtrieve Oxidation of 4-Chlorobenzyl Alcohol. Experiment 13. The Sodium Borohydride Reduction of Benzil and Benzoin. Experiment 14. The Grignard Reaction: The Preparation of 1,1-Diphenylethanol. Experiment 15. The Asymmetric Dihydroxylation of trans-stilbene. -Pinene Experiment 16. Some Chemistry of Oxide. Experiment 17. A Dehydrogenation/ Hydrogenation Reaction. Experiment 18. The Friedel- Crafts Reaction. Experiment 19. Microwave Heating of Organic Compounds. Experiment 20. The Reaction of 1,1-Diphenylethanol on Clay in the Presence of Microwave Radiation. Experiment 21. The Wittig Reaction. Experiment 22. The Suzuki Reaction. Experiment 23. The Crossed-Aldol Condensation. Experiment 24. Identifying the Structure of an Aldehyde by Qualitative Analysis. Experiment 25. The Benzoin Reaction. Experiment 26. The Diels-Alder Reaction. Experiment 27. -ß-Unsaturated Carboxylic Acid Derivative.Synthesis of an Experiment 28. The Reaction of 2-Acetylphenyl Benzoate with Potassium Hydroxide. Experiment 29. The Reaction of 2-Acetylphenyl Benzoate with Potassium Hydroxide. Experiment 30. Synthesis of 1,2,3,4-Tetrahydro-â-Carboline. Experiment 31. Base-Catalyzed Hydrolysis of Nicotinonitrile Using an Anion-Exchange Resin. Experiment 32. Reactions of Salicylamide. Experiment 33. The Hunsdiecker Reaction. Experiment 34. The Investigation of the Mechanism of a Reaction. Experiment 35. Monoterpenes and the Ritter Reaction. Experiment 36. Chemoselectivity in Transfer- Hydrogenation Reactions. 2011, 526pp, Paperback, 9781111428174 Physical Chemistry PHYSICAL CHEMISTRY, 4E Keith J. Laidler, University of Ottawa; John H. Meiser, Ball State University; Bryan C. Sanctuary, McGill University With its clear explanations and practical pedagogy, Physical Chemistry is less intimidating to students than other texts, without sacrificing the mathematical rigor and comprehensiveness necessary for a junior-level physical chemistry course. The text s long-standing reputation for accessible writing provides clear instruction and superior problem-solving support for students. Note: Each chaper concludes with Key Equations, Problems, and Suggested Reading. 1. The Nature of Physical Chemistry and the Kinetic Theory of Gases 1.1 The Nature of Physical Chemistry 1.2 Some Concepts from Classical Mechanics 1.3 Systems, States, and Equilibrium 1.4 Thermal Equilibrium 1.5 Pressure and Boyle s Law Biography: Robert Boyle 1.6 Gay-Lussac s (Charles s) Law 1.7 The Ideal Gas Thermometer 1.8 The Equation of State for an Ideal Gas 1.9 The Kinetic-Molecular Theory of Ideal Gases 1.10 The Barometric Distribution Law 1.11 The Maxwell Distribution of Molecular Speeds and Translational Energies 1.12 Real Gases 1.13 Equations of State 1.14 The Virial Equation Appendix: Some Definite and Indefinite Integrals Often Used in Physical Chemistry 2. The First Law of Thermodynamics 2.1 Origins of the First Law 2.2 States and State Functions 2.3 Equilibrium States and Reversibility 2.4 Energy, 111

Heat, and Work 2.5 Thermochemistry 2.6 Ideal Gas Relationships 2.7 Real Gases 3. The Second and Third Laws of Thermodynamics Biography: Rudolph Julius Emmanuel Clausius 3.1 The Carnot Cycle 3.2 Irreversible Processes 3.3 Molecular Interpretation of Entropy 3.4 The Calculation of Entropy Changes 3.5 The Third Law of Thermodynamics 3.6 Conditions for Equilibrium 3.7 The Gibbs Energy 3.8 Some Thermodynamic Relationships 3.9 The Gibbs-Helmholtz Equation 3.10 Thermodynamic Limitations to Energy Conversion 4. Chemical Equilibrium Biography: Jacobus Henricus van t Hoff 4.1 Chemical Equilibrium Involving Ideal Gases 4.2 Equilibrium in Nonideal Gaseous Systems 4.3 Chemical Equilibrium in Solution 4.4 Heterogeneous Equilibrium 4.5 Tests for Chemical Equilibrium 4.6 Shifts of Equilibrium at Constant Temperature 4.7 Coupling of Reactions 4.8 Temperature Dependence of Equilibrium Constants 4.9 Pressure Dependence of Equilibrium Constants 5. Phases and Solutions 5.1 Phase Recognition 5.2 Vaporization and Vapor Pressure 5.3 Classification of Transitions in Single-Component Systems 5.4 Ideal Solutions: Raoult s and Henry s Laws 5.5 Partial Molar Quantities 5.6 The Chemical Potential 5.7 Thermodynamics of Solutions 5.8 The Colligative Properties 6. Phase Equilibria 6.1 Equilibrium Between Phases 6.2 One-Component Systems 6.3 Binary Systems Involving Vapor 6.4 Condensed Binary Systems 6.5 Thermal Analysis 6.6 More Complicated Binary Systems 6.7 Crystal Solubility: The Krafft Boundary and Krafft Eutectic 6.8 Ternary Systems 7. Solutions of Electrolytes 7.1 Faraday s Laws of Electrolysis Biography: Michael Faraday 7.2 Molar Conductivity 7.3 Weak Electrolytes: The Arrhenius Theory Biography: Svante August Arrhenius 7.4 Strong Electrolytes 7.5 Independent Migration of Ions 7.6 Transport Numbers 7.7 Ion Conductivities 7.8 Thermodynamics of Ions 7.9 Theories of Ions in Solution 7.10 Activity Coefficients 7.11 Ionic Equilibria 7.12 Ionization of Water 7.13 The Donnan Equilibrium 8. Electrochemical Cells 8.1 The Daniell Cell 8.2 Standard Electrode Potentials 8.3 Thermodynamics of Electrochemical Cells 8.4 Types of Electrochemical Cells 8.5 Applications of emf Measurements 8.6 Fuel Cells 8.7 Photogalvanic Cells 8.8 Batteries, Old and New 9. Chemical Kinetics I. The Basic Ideas 9.1 Rates of Consumption and Formation 9.2 Rate of Reaction 9.3 Empirical Rate Equations 9.4 Analysis of Kinetic Results 9.5 Techniques for Very Fast Reactions 9.6 Molecular Kinetics 9.7 The Arrhenius Equation 9.8 Potential-Energy Surfaces 9.9 The Preexponential Factor Biography: Henry Eyring 9.10 Reactions in Solution 9.11 Reaction Dynamics 10. Chemical Kinetics II. Composite Mechanisms 10.1 Evidence for a Composite Mechanism 10.2 Types of Composite Reactions 10.3 Rate Equations for Composite Mechanisms 10.4 Rate Constants, Rate Coefficients, and Equilibrium Constants 10.5 Free-Radical Reactions 10.6 Photochemical Reactions 10.7 Radiation-Chemical Reactions 10.8 Explosions 10.9 Catalysis 10.10 Reactions in Solution: Some Special Features 10.11 Mechanisms of Polymerization in Macromolecules 10.12 Kinetics of Polymerization 10.13 Induction Periods, Oscillations, and Chaos 10.14 Electrochemical Dynamics 11. Quantum Mechanics and Atomic Structure 11.1 Electromagnetic Radiation and the Old Quantum Theory 11.2 Bohr s Atomic Theory 11.3 The Foundations of Quantum Mechanics 11.4 Schrödinger s Wave Mechanics 11.5 Quantum-Mechanical Postulates 11.6 Quantum Mechanics of Some Simple Systems 11.7 Quantum Mechanics of Hydrogenlike Atoms 11.8 Physical Significance of the Orbital Quantum Numbers 11.9 Angular Momentum and Magnetic Moment 11.10 The Rigid Linear Rotor 11.11 Spin Quantum Numbers 11.12 Many-Electron Atoms 11.13 Approximate Methods in Quantum Mechanics 12. The Chemical Bond Biography: Gilbert Newton Lewis 12.1 The Hydrogen Molecular- Ion, H2+ 12.2 The Hydrogen Molecule 12.3 Hückel Theory for More Complex Molecules 12.4 Valence-Bond Theory for More Complex Molecules 12.5 Symmetry in Chemistry 12.6 Symmetry of Molecular Orbitals Appendix: Character Tables 13. Foundations of Chemical Spectroscopy 13.1 Emission and Absorption Spectra 13.2 Atomic Spectra Biography: Gerhard Herzberg 13.3 Pure Rotational Spectra of Molecules 13.4 Vibrational- Rotational Spectra of Molecules 13.5 Raman Spectra 13.6 Electronic Spectra of Molecules Appendix: Symmetry Species Corresponding to Infrared and Raman Spectra 14. Some Modern Applications of Spectroscopy 14.1 Laser Spectroscopy 14.2 Spectral Line Widths 14.3 Types of Lasers 14.4 Laser Techniques for Chemistry 14.5 Magnetic Spectroscopy 14.6 Nuclear Magnetic Spectroscopy 14.7 Electron Magnetic Resonance (EMR) 14.8 Mössbauer Spectroscopy 14.9 Photoelectron Spectroscopy 14.10 Photoacoustic Spectroscopy 14.11 Chiroptical Methods 14.12 Mass Spectrometry 15. Statistical Mechanics 15.1 Forms of Molecular Energy Biography: Ludwig Boltzmann 15.2 Principles of Statistical Mechanics 15.3 The Partition Function 15.4 Thermodynamic Quantities from Partition Functions 15.5 The Partition Function for Some Special Cases 112

15.6 The Internal Energy, Enthalpy, and Gibbs Energy Functions 15.7 The Calculation of Equilibrium Constants 15.8 Transition-State Theory 15.9 The Approach to Equilibrium 15.10 The Canonical Ensemble 16. The Solid State 16.1 Crystal Forms and Crystal Lattices 16.2 X-Ray Crystallography 16.3 Experimental Methods Biography: Dorothy Crowfoot Hodgkin 16.4 Theories of Solids 16.5 Statistical Thermodynamics of Crystals: Theories of Heat Capacities 16.6 Electrical Conductivity in Solids 16.7 Optical Properties of Solids 17. The Liquid State 17.1 Liquids Compared with Dense Gases 17.2 Liquids Compared with Solids 17.3 Intermolecular Forces 17.4 Theories and Models of Liquids 17.5 Water, the Incomparable Liquid 17.6 The Hydrophobic Effect 18. Surface Chemistry and Colloids 18.1 Adsorption 18.2 Adsorption Isotherms 18.3 Thermodynamics and Statistical Mechanics of Adsorption 18.4 Chemical Reactions on Surfaces 18.5 Surface Heterogeneity 18.6 The Structure of Solid Surfaces and of Adsorbed Layers 18.7 Surface Tension and Capillarity 18.8 Liquid Films on Surfaces Biography: Agnes Pockels 18.9 Colloidal Systems 19. Transport Properties 19.1 Viscosity 19.2 Diffusion 19.3 Sedimentation Appendix A Units, Quantities, and Symbols: The SI/IUPAC Recommendations Appendix B Physical Constants Appendix C Some Mathematical Relationships Appendix D Standard Enthalpies, Entropies, and Gibbs Energies of Formation Appendix E Character Tables for Some Important Symmetry Groups in Chemistry Answers to Problems Index 2003, 1088pp, Hardback, 9780618123414 PHYSICAL CHEMISTRY, 2E David W. Ball, Cleveland State University Coming Soon! With its easy-to-read approach and focus on core topics, PHYSICAL CHEMISTRY, 2e provides a concise, yet thorough examination of calculus-based physical chemistry. The Second Edition, designed as a learning tool for students who want to learn physical chemistry in a functional and relevant way, follows a traditional organization and now features an increased focus on thermochemistry, as well as new problems, new two-column examples, and a dynamic new four-color design. Written by a dedicated chemical educator and researcher, the text also includes a review of calculus applications as applied to physical chemistry. NEW TO THIS EDITION Chapters 1-8 have been completely revised for a better examination of the principles of thermochemistry. Design and art have been upgraded from a static 2-color display to a dynamic 4-color design. This edition s dynamic, four-color art and photo program fully complements the text and visually reinforces students conceptual understanding. New two-column in-text examples, where appropriate, provide students with more explanation on how to work problems and apply key concepts. An increased number of end-of-chapter problems provide a wider variety of difficulty. A stronger thermochemistry presence appears throughout the entire book, not just in Chapters 1-8. Chapter 9, Pre-Quantum Mechanics, a unique preview to Quantum Mechanics, allows students to develop a better understanding of the importance, conclusions, and necessity of the subject by putting the state of classical science into a historical context. The text covers the core concepts of physical chemistry in great detail, foregoing coverage of topics rarely covered in an undergraduate physical chemistry course. A large number of worked examples with varying degrees of difficulty are integrated throughout the text to promote students understanding of concepts and the development of chemical problem-solving skills, Written in a two-column format, many of these examples now have further explanation and commentary. Although there are some mathematical derivations among the exercises, most exercises have been created with an emphasis on asking students to use the concepts, rather than just derive them. Because of the text s emphasis on understanding physical 113

chemistry concepts, many examples are conceptual in nature. An equal emphasis is placed on both units and numbers in examples and subsequent exercises and problems. End-of-chapter exercises and problems vary in complexity and difficulty, allowing instructors a broader range to choose from. 1. Gases and the Zeroth Law of Thermodynamics. 2. The First Law of Thermodynamics. 3. The Second and Third Laws of Thermodynamics. 4. Free Energy and Chemical Potential. 5. Introduction to Chemical Equilibrium. 6. Equilibria in Single-Component Systems. 7. Equilibria in Multiple-Component Systems. 8. Electrochemistry and Ionic Solutions. 9. Pre-Quantum Mechanics. 10. Introduction to Quantum Mechanics. 11. Quantum Mechanics: Model Systems and the Hydrogen Atom. 12. Atoms and Molecules. 13. Introduction to Symmetry in Quantum Mechanics. 14. Rotational and Vibrational Spectroscopy. 15. Introduction to Electronic Spectroscopy and Structure. 16. Introduction to Magnetic Spectroscopy. 17. Statistical Thermodynamics: Introduction. 18. More Statistical Thermodynamics. 19. The Kinetic Theory of Gases. 20. Kinetics. 21. The Solid State: Crystals. 22. Surfaces. Appendixes. Answers to Selected Exercises. Index. 2015, 880pp, Hardback, 9781133958437 Spectroscopy Coming Soon! INTRODUCTION TO SPECTROSCOPY, INTERNATIONAL EDITION, 4E Donald L. Pavia, Western Washington University; Gary M. Lampman, Western Washington University Introduce your students to the latest advances in spectroscopy with the text that has set the unrivaled standard for more than 30 years: Pavia/Lampman s SPECTROSCOPY, 4e, International Edition. Whether you use this comprehensive resource as the primary text in an upper-level spectroscopy course or as a companion book with an organic chemistry text, your students receive an unmatched systematic introduction to spectra and basic theoretical concepts in spectroscopic methods. This well-rounded introduction to spectroscopy features updated spectra; a modernized presentation of one-dimensional nuclear magnetic resonance (NMR) spectroscopy; the introduction of biological molecules in mass spectrometry; and inclusion of modern techniques alongside DEPT, COSY, and HECTOR. NEW TO THIS EDITION ADDITION OF MODERN PROCESSES: Additional techniques in Chapter 6 modernize this edition s presentation on one-dimensional NMR spectroscopy. EXPANDED COVERAGE WITHIN MASS SPECTROMETRY: The mass spectrometry material (Chapter 8) now provides a detailed look at biological molecules for the latest coverage on this important topic. NEWEST SPECTRA TECHNIQUES: You can easily provide students with the latest spectra techniques, found in Appendix 10, Index of Spectra. EXTENSIVELY UPDATED SPECTROGRAPHS: 114

Throughout the text, new spectrographs have been created with updated techniques to improve accuracy and presentation. PROVEN RESOURCE AND REFERENCE TEXT: This book has been recognized for more than 30 years as an excellent resource for the spectroscopy student and anyone seeking a solid introductory reference text on spectroscopy. 1. Molecular Formulas and What Can Be Learned From Them. 2. Infrared Spectroscopy. 3. Nuclear Magnetic Resonance Spectroscopy Part One: Basic Concepts. 4. Nuclear Magnetic Resonance Spectroscopy Part Two: Carbon-13 Spectra, Including Heteronuclear Coupling With Other Nuclei. 5. Nuclear Magnetic Resonance Spectroscopy Part Three: Spin-Spin Coupling. 6. Nuclear Magnetic Resonance Spectroscopy Part Four: Other Topics in One-Dimensional NMR. 7. Ultraviolet Spectroscopy. 8. Mass Spectrometry. 9. Combined Structure Problems. 10. Nuclear Magnetic Resonance Spectroscopy Part Five: Advanced NMR Techniques. Answers to Selected Problems. Appendix 1: Infrared Absorption Frequencies of Functional Groups. Appendix 2: Some Representative Chemical Shift Values for Various Types of Protons. Appendix 3: Typical Proton Coupling Constants. Appendix 4: Calculation of Proton (1H) Chemical Shifts. Appendix 5: Calculation of Carbon-13 Chemical Shifts. Appendix 6: 13C Coupling Constants. Appendix 7: Tables of Precise Masses and Isotopic Abundance Ratios for Molecular Ions Under Mass 100 Containing Carbon, Hydrogen, Nitrogen, and Oxygen. Appendix 8: Common Fragment Ions Under Mass 105. Appendix 9: Handy-Dandy Guide to Mass Spectral Fragmentation Patterns. Appendix 10: Index of Spectra. Index. 2009, 736pp, Paperback, 9780538734189 115

Combined Author/Title Index A A Beginner s Guide to Scientific Method, International Edition, 4e, p.30/p.62 A Microscale Approach to Organic Laboratory Techniques, International Edition, 5e, p.83 A Small Scale Approach to Organic Laboratory Techniques, 3e, p.85 Abd Rahman/Mohamed Jelan/Sulaiman, Chemistry for Matriculation, p.42 Applications of Microsoft Excel in Analytical Chemistry, 2e, p.23 Armstrong, General, Organic, and Biochemistry, p.2 Atwood, Survival Guide for General Chemistry with Math Review, 2e, p.60/p.80 Atwood, Survival Guide for Introductory Chemistry, p.80 B Ball, Essential Algebra for Chemistry Students, 2e, p.45/p.67 Ball, Physical Chemistry, 2e, p.113 Basic Chemistry, 7e, p.63 Basic Chemistry, 8e, p.65 Basic Laboratory Experiments for General, Organic, and Biochemistry, p.2 Bauer/Birk/Sawyer, Laboratory Inquiry in Chemistry, 3e, p.52 Bee Lee/Yew Lee/Chui Yean/Sivaneson, Chemistry For SPM, p.67 Bettelheim/Brown/Campbell/Farrell, Introduction to General, Organic and Biochemistry, International Edition, 10e, p.9 Bettelheim/Brown/Campbell/Farrell, Introduction to Organic and Biochemistry, 8e, p.10 Bettelheim/Landesberg, Laboratory Experiments for Introduction to General, Organic and Biochemistry, International Edition, 8e, p.14 Biochemistry, International Edition, 5e, p.28 Biochemistry, International Edition, 7e, p.27 Bishop/Bishop/Whitten, Standard and Microscale Experiments in General Chemistry, 5e, p.58 Block/McKelvy, Lab Experiments for General Chemistry, 5e, p.51 Boikess, Chemical Principles for Organic Chemistry, p.88 Brown/Holme, Chemistry for Engineering Students, International Edition, 2e, p.41 Brown/Iverson/Anslyn/Foote, Organic Chemistry, International Edition, 7e, p.103 Brown/Iverson/Anslyn/Foote, Study Guide with Solutions Manual for Brown/Iverson/Anslyn/Foote s Organic Chemistry, 7th, 7e, p.108 C CHEM 4LTR (with Review Cards and Chemistry CourseMate with ebook Printed Access Card), p.82 Campbell/Farrell, Biochemistry, International Edition, 7e, p.27 Carey, A Beginner s Guide to Scientific Method, International Edition, 4e, p.30/p.62 Chem 2, 2e, p.81 Chemical Principles for Organic Chemistry, p.88 Chemical Principles in the Laboratory, International Edition, 10e, p.32 Chemical Principles, 7e, p.31 Chemistry, p.37 Chemistry & Chemical Reactivity, AP* Edition, 8e, p.38 Chemistry 2012 Update, AP* Edition, 8e, p.39 Chemistry For SPM, p.67 Chemistry and Chemical Reactivity, International Edition, 8e, p.39 Chemistry for Engineering Students, International Edition, 2e, p.41 Chemistry for Matriculation, p.42 Chemistry with CB CourseSmart ebook, 9e, p.42 Chemistry, 3e, p.34 Chemistry, 4e, p.36 Chemistry, 7e, p.33/p.34 Chemistry, International Edition, 10e, p.44 Cracolice/Peters, Introductory Chemistry, 5e, p.77 D DeCoste, Study Guide for Zumdahl/DeCoste s Introductory Chemistry: A Foundation, 8th, 8e, p.79 Descriptive Inorganic, Coordination, and Solid State Chemistry, International Edition, 3e, p.61 E Ebbing/Gammon, General Chemistry, International Edition, 10e, p.49 Ebbing/Gammon, Study Guide for Ebbing/Gammon s General Chemistry, 10th, 10e, p.59 Engel/Kriz/Lampman/Pavia, Introduction to Organic Laboratory Techniques, 3e, p.91 Essential Algebra for Chemistry Students, 2e, p.45/p.67 Experimental Organic Chemistry, 5e, p.89 Experiments in General Chemistry, 5e, p.47 Experiments in General Chemistry, 6e, p.46 Experiments in General Chemistry, Lab Manual, 10e, p.48 Experiments in General Chemistry: Inquiry and Skill Building, 2e, p.48 F Fundamentals of Analytical Chemistry, International Edition, 9e, p.24 Fundamentals of Organic Chemistry, International Edition, 7e, p.90 G Garrett/Grisham, Biochemistry, International Edition, 5e, p.28 Garrett/Grisham, Study Guide with Student Solutions Manual and Problems Book for Garrett/Grisham s Biochemistry, 5th, 5e, p.29 General, Organic, and Biochemistry, p.2 General, Organic, and Biological Chemistry, International Edition, 6e, p.4 Guided Explorations in General Chemistry, 2e, p.50 H Hanson, Guided Explorations in General Chemistry, 2e, p.50 Hart/Hadad/Craine/Hart, Organic Chemistry, 13e, p.98/p.99 Hogg, Chem 2, 2e, p.81 116

Combined Author/Title Index Holler/Crouch, Applications of Microsoft Excel in Analytical Chemistry, 2e, p.23 I Inquiry Based Learning Guide for Zumdahl/Zumdahl s Chemistry, 9th, 9e, p.51 Introduction To Analytical Chemistry, p.25 Introduction to Basic Chemistry, International Edition, 7e, p.68 Introduction to Chemical Principles, 7e, p.70 Introduction to Chemistry, 7e, p.71 Introduction to General, Organic and Biochemistry, International Edition, 10e, p.9 Introduction to Organic Laboratory Techniques, 3e, p.91 Introduction to Organic and Biochemistry, 8e, p.10 Introduction to Spectroscopy, International Edition, 4e, p.114 Introductory Chemistry for Today, International Edition, 7e, p.11 Introductory Chemistry for Today, International Edition, 8e, p.12 Introductory Chemistry, 5e, p.77 Introductory Chemistry, 7e, p.74 Introductory Chemistry, 8e, p.78 J Jaafar/Lim You Sie, Organic Chemistry for Matriculation, p.54 Joesten/Hogg/Donald R. Neu, CHEM 4LTR (with Review Cards and Chemistry CourseMate with ebook Printed Access Card), p.82 K Kotz/Treichel/Townsend, Chemistry & Chemical Reactivity, AP* Edition, 8e, p.38 Kotz/Treichel/Townsend, Chemistry and Chemical Reactivity, International Edition, 8e, p.39 L Lab Experiments for General Chemistry, 5e, p.51 Lab Manual for Zumdahl/DeCoste s Introductory Chemistry: A Foundation, 8th, 8e, p.79 Lab Manual for Zumdahl/Zumdahl s Chemistry, 9th, 9e, p.52 Laboratory Experiments for Introduction to General, Organic and Biochemistry, International Edition, 8e, p.14 Laboratory Inquiry in Chemistry, 3e, p.52 Laidler/Meiser/Sanctuary, Physical Chemistry, 4e, p.111 Landesberg, Basic Laboratory Experiments for General, Organic, and Biochemistry, p.2 Little, Lab Manual for Zumdahl/DeCoste s Introductory Chemistry: A Foundation, 8th, 8e, p.79 M Macroscale and Microscale Organic Experiments, 6e, p.94 Martin/Gilbert, Experimental Organic Chemistry, 5e, p.89 Masterton/Hurley/Neth, Chemistry, 7e, p.33/p.34 McMurry, Fundamentals of Organic Chemistry, International Edition, 7e, p.90 McMurry, Organic Chemistry with Biological Applications, 3e, p.101 McMurry, Organic Chemistry, 2e, p.95/p.96 McMurry, Organic Chemistry, International Edition, 8e, p.105 McMurry, Study Guide with Solutions Manual for McMurry s Organic Chemistry: With Biological Applications, 3rd, 3e, p.108 McMurry, Study Guide with Student Solutions Manual for McMurry s Organic Chemistry, 8th, 8e, p.109 Microscale Experiments for General Chemistry, p.53 Moore/Stanitski/Jurs, Chemistry, 4e, p.36 Moore/Stanitski/Jurs, Principles of Chemistry, p.54 Murov, Experiments in General Chemistry, 5e, p.47 Murov, Experiments in General Chemistry, 6e, p.46 O Organic Chemistry, p.100/p.101 Organic Chemistry for Matriculation, p.54 Organic Chemistry with Biological Applications, 3e, p.101 Organic Chemistry, 13e, p.98/p.99 Organic Chemistry, 2e, p.95/p.96 Organic Chemistry, International Edition, 7e, p.103 Organic Chemistry, International Edition, 8e, p.105 Organic Experiments, 6e, p.106 Organic and Biochemistry for Today, International Edition, 7e, p.15 Organic and Biochemistry for Today, International Edition, 8e, p.16 Organic and Biological Chemistry, 6e, p.17 Oxtoby/Gillis/Campion, Principles of Modern Chemistry, International Edition, 7e, p.56 P Pavia/Kriz/Lampman/Engel, A Microscale Approach to Organic Laboratory Techniques, International Edition, 5e, p.83 Pavia/Lampman, Introduction to Spectroscopy, International Edition, 4e, p.114 Pavia/Lampman/Kriz/Engel, A Small Scale Approach to Organic Laboratory Techniques, 3e, p.85 Pedersen/Myers, Understanding the Principles of Organic Chemistry, p.110 Physical Chemistry, 2e, p.113 Physical Chemistry, 4e, p.111 Principles of Chemistry, p.54 Principles of Modern Chemistry, International Edition, 7e, p.56 Pushing Electrons, 4e, p.107 R Reger/Goode/Ball, Chemistry, 3e, p.34 Rodgers, Descriptive Inorganic, Coordination, and Solid State Chemistry, International Edition, 3e, p.61 S Safety-Scale Laboratory Experiments for Chemistry for Today, 7e, p.21 Safety-Scale Laboratory Experiments for Chemistry for Today, 8e, p.22 Sanger, Study Guide for Moore/Stanitski s Chemistry: The Molecular Science, 5th, 5e, p.60 Seager/Slabaugh, Introductory Chemistry for Today, International Edition, 7e, p.11 117

Combined Author/Title Index Seager/Slabaugh, Introductory Chemistry for Today, International Edition, 8e, p.12 Seager/Slabaugh, Organic and Biochemistry for Today, International Edition, 7e, p.15 Seager/Slabaugh, Organic and Biochemistry for Today, International Edition, 8e, p.16 Seager/Slabaugh, Safety-Scale Laboratory Experiments for Chemistry for Today, 7e, p.21 Seager/Slabaugh, Safety-Scale Laboratory Experiments for Chemistry for Today, 8e, p.22 Seager/Slabaugh, Study Guide with Student Solutions Manual for Seager/Slabaugh s Chemistry for Today, 8th, 8e, p.22 Skoog and West s Fundamentals of Analytical Chemistry, 9e, p.26 Skoog/West/Holler/Crouch, Fundamentals of Analytical Chemistry, International Edition, 9e, p.24 Skoog/West/Holler/Crouch, Introduction To Analytical Chemistry, p.25 Skoog/West/Holler/Crouch, Skoog and West s Fundamentals of Analytical Chemistry, 9e, p.26 Slowinski/Wolsey/Rossi, Chemical Principles in the Laboratory, International Edition, 10e, p.32 Standard and Microscale Experiments in General Chemistry, 5e, p.58 Stoker, General, Organic, and Biological Chemistry, International Edition, 6e, p.4 Stoker, Organic and Biological Chemistry, 6e, p.17 Straumanis, Organic Chemistry, p.100/p.101 Study Guide for Ebbing/Gammon s General Chemistry, 10th, 10e, p.59 Study Guide for Moore/Stanitski s Chemistry: The Molecular Science, 5th, 5e, p.60 Study Guide for Whitten/Davis/Peck/Stanley s Chemistry, 10th, 10e, p.60 Study Guide for Zumdahl/DeCoste s Introductory Chemistry: A Foundation, 8th, 8e, p.79 Study Guide for Zumdahl/Zumdahl s Chemistry, 9th, 9e, p.60 Study Guide with Solutions Manual for Brown/Iverson/Anslyn/ Foote s Organic Chemistry, 7th, 7e, p.108 Study Guide with Solutions Manual for McMurry s Organic Chemistry: With Biological Applications, 3rd, 3e, p.108 Study Guide with Student Solutions Manual and Problems Book for Garrett/Grisham s Biochemistry, 5th, 5e, p.29 Study Guide with Student Solutions Manual for McMurry s Organic Chemistry, 8th, 8e, p.109 Study Guide with Student Solutions Manual for Seager/ Slabaugh s Chemistry for Today, 8th, 8e, p.22 Survival Guide for General Chemistry with Math Review, 2e, p.60/p.80 Survival Guide for Introductory Chemistry, p.80 W Weeks, Pushing Electrons, 4e, p.107 Weiner/Harrison, Introduction to Chemical Principles, 7e, p.70 Wentworth/Munk, Experiments in General Chemistry, Lab Manual, 10e, p.48 Whitten/Davis/Peck/Stanley, Chemistry, International Edition, 10e, p.44 Whitten/Davis/Peck/Stanley, Study Guide for Whitten/Davis/ Peck/Stanley s Chemistry, 10th, 10e, p.60 Williamson/Little, Microscale Experiments for General Chemistry, p.53 Williamson/Masters, Macroscale and Microscale Organic Experiments, 6e, p.94 Williamson/Masters, Organic Experiments, 6e, p.106 Williamson/Masters, Techniques Labs for Macroscale and Microscale Organic Experiments (with CourseMate 2-Semester Printed Access Card), 6e, p.109 Williamson/Peck, Experiments in General Chemistry: Inquiry and Skill Building, 2e, p.48 Z Zumdahl/DeCoste, Basic Chemistry, 7e, p.63 Zumdahl/DeCoste, Basic Chemistry, 8e, p.65 Zumdahl/DeCoste, Chemical Principles, 7e, p.31 Zumdahl/DeCoste, Introduction to Basic Chemistry, International Edition, 7e, p.68 Zumdahl/DeCoste, Introduction to Chemistry, 7e, p.71 Zumdahl/DeCoste, Introductory Chemistry, 7e, p.74 Zumdahl/DeCoste, Introductory Chemistry, 8e, p.78 Zumdahl/Zumdahl, Chemistry, p.37 Zumdahl/Zumdahl, Chemistry 2012 Update, AP* Edition, 8e, p.39 Zumdahl/Zumdahl, Chemistry with CB CourseSmart ebook, 9e, p.42 Zumdahl/Zumdahl, Inquiry Based Learning Guide for Zumdahl/Zumdahl s Chemistry, 9th, 9e, p.51 Zumdahl/Zumdahl, Lab Manual for Zumdahl/Zumdahl s Chemistry, 9th, 9e, p.52 Zumdahl/Zumdahl, Study Guide for Zumdahl/Zumdahl s Chemistry, 9th, 9e, p.60 T Techniques Labs for Macroscale and Microscale Organic Experiments (with CourseMate 2-Semester Printed Access Card), 6e, p.109 U Understanding the Principles of Organic Chemistry, p.110 118

ORDER FORM / PRICE LIST QTY YEAR ISBN NO. AUTHOR TITLE/EDITION PAGE NO. PRICE(USD) A 2012 9781111726010 Carey A Beginner s Guide to Scientific Method, International Edition, 4e 2013 9781133107415 Pavia A Microscale Approach to Organic Laboratory Techniques, International Edition, 5e 2011 9781439049327 Pavia A Small Scale Approach to Organic Laboratory Techniques, 3e 2014 9781285087955 Holler Applications of Microsoft Excel in Analytical Chemistry, 2e B p.30/p.62 87.95 p.83 332.95 p.85 309.95 p.23 80.95 2011 9780538736374 Zumdahl Basic Chemistry, 7e p.63 205.95 2015 9781285453149 Zumdahl Basic Chemistry, 8e p.65 205.95 2012 9781111426613 Landesberg Basic Laboratory Experiments for General, Organic, and Biochemistry p.2 86.95 2013 9781133108795 Garrett Biochemistry, International Edition, 5e p.28 365.95 2012 9781111425647 Campbell Biochemistry, International Edition, 7e p.27 276.95 C 2015 9781133962984 Hogg Chem 2, 2e p.81 89.95 2011 9780538738217 Joesten CHEM 4LTR (with Review Cards and Chemistry CourseMate with ebook Printed Access Card) p.82 82.95 2015 9781285457697 Boikess Chemical Principles for Organic Chemistry p.88 46.95 2012 9781111576608 Slowinski Chemical Principles in the Laboratory, International Edition, 10e p.32 205.95 2013 9781111580650 Zumdahl Chemical Principles, 7e p.31 314.95 2012 9780840065865 Zumdahl Chemistry p.37 301.95 2012 9781111427047 Kotz Chemistry & Chemical Reactivity, AP* Edition, 8e p.38 185.95 2012 9781111577346 Zumdahl Chemistry 2012 Update, AP* Edition, 8e p.39 185.95 2012 9781111427023 Kotz Chemistry and Chemical Reactivity, International Edition, 8e 2011 9780538733649 Brown Chemistry for Engineering Students, International Edition, 2e p.39 343.95 p.41 289.95 2006 9789812544247 Abd Rahman Chemistry for Matriculation p.42 39.95 2011 9789671014400 Bee Lee Chemistry For SPM p.67 30.50 2014 9789814568715 Zumdahl Chemistry with CB CourseSmart ebook, 9e p.42 336.95 2010 9780495559832 Reger Chemistry, 3e p.34 329.95 2011 9781439049662 Moore Chemistry, 4e p.36 330.95 2012 9781111572174 Masterton Chemistry, 7e p.33 273.95 2012 9781111572587 Masterton Chemistry, 7e p.34 151.95 2014 9781133933595 Whitten Chemistry, International Edition, 10e p.44 343.95 Prices quoted here are correct at time of printing and are subject to change without prior notice

QTY YEAR ISBN NO. AUTHOR TITLE/EDITION PAGE NO. PRICE(USD) D 2012 9781111427153 Rodgers Descriptive Inorganic, Coordination, and Solid State Chemistry, International Edition, 3e E p.61 295.95 2006 9780495013273 Ball Essential Algebra for Chemistry Students, 2e p.45/p.67 51.95 2011 9781439049167 Martin Experimental Organic Chemistry, 5e p.89 305.95 2007 9780495125389 Murov Experiments in General Chemistry, 5e p.47 191.95 2015 9781285458540 Murov Experiments in General Chemistry, 6e p.46 187.95 2013 9781111989422 Wentworth Experiments in General Chemistry, Lab Manual, 10e p.48 179.95 2014 9781285433172 Williamson Experiments in General Chemistry: Inquiry and Skill Building, 2e F 2014 9781285056241 Skoog Fundamentals of Analytical Chemistry, International Edition, 9e 2011 9781439049730 McMurry Fundamentals of Organic Chemistry, International Edition, 7e G p.48 134.95 p.24 351.95 p.90 283.95 2013 9781111989491 Ebbing General Chemistry, International Edition, 10e p.49 343.95 2012 9780840068286 Armstrong General, Organic, and Biochemistry p.2 169.95 2013 9781133106869 Stoker General, Organic, and Biological Chemistry, International Edition, 6e p.4 300.95 2011 9781439049655 Hanson Guided Explorations in General Chemistry, 2e p.50 102.95 I 2014 9781133611523 Zumdahl Inquiry Based Learning Guide for Zumdahl/Zumdahl s Chemistry, 9th, 9e p.50 41.95 2011 9789814272797 Skoog Introduction To Analytical Chemistry p.25 129.95 2011 9780538736640 Zumdahl Introduction to Basic Chemistry, International Edition, 7e p.68 205.95 2010 9781439046647 Weiner Introduction to Chemical Principles, 7e p.70 191.95 2011 9780538735438 Zumdahl Introduction to Chemistry, 7e p.71 239.95 2013 9781133109112 Bettelheim Introduction to General, Organic and Biochemistry, International Edition, 10e p.9 300.95 2013 9781133109761 Bettelheim Introduction to Organic and Biochemistry, 8e p.10 257.95 2011 9780538733281 Engel Introduction to Organic Laboratory Techniques, 3e p.91 309.95 2009 9780538734189 Pavia Introduction to Spectroscopy, International Edition, 4e p.114 310.95 2011 9780538734868 Seager Introductory Chemistry for Today, International Edition, 7e p.11 231.95 2014 9781133605119 Seager Introductory Chemistry for Today, International Edition, 8e p.12 266.95 2013 9781133108115 Cracolice Introductory Chemistry, 5e p.77 252.95 2011 9780538736398 Zumdahl Introductory Chemistry, 7e p.74 207.95 2015 9781285453132 Zumdahl Introductory Chemistry, 8e p.78 207.95 L 2006 9780534424480 Block Lab Experiments for General Chemistry, 5e p.51 205.95 2015 9781285845166 Little Lab Manual for Zumdahl/DeCoste s Introductory Chemistry: A Foundation, 8th, 8e p.79 149.95 Prices quoted here are correct at time of printing and are subject to change without prior notice

QTY YEAR ISBN NO. AUTHOR TITLE/EDITION PAGE NO. PRICE(USD) 2014 9781133611486 Zumdahl Lab Manual for Zumdahl/Zumdahl s Chemistry, 9th, 9e p.52 179.95 2013 9781133113102 Bettelheim Laboratory Experiments for Introduction to General, Organic and Biochemistry, International Edition, 8e p.14 188.95 2009 9780495113454 Bauer Laboratory Inquiry in Chemistry, 3e p.52 116.95 M 2011 9780538733335 Williamson Macroscale and Microscale Organic Experiments, 6e p.94 288.95 1997 9780669416060 Williamson Microscale Experiments for General Chemistry p.53 181.95 O 2011 9780538734851 Seager Organic and Biochemistry for Today, International Edition, 7e 2014 9781133607496 Seager Organic and Biochemistry for Today, International Edition, 8e p.15 242.95 p.16 266.95 2013 9781133103950 Stoker Organic and Biological Chemistry, 6e p.17 245.95 2012 9781111578299 Straumanis Organic Chemistry p.101 29.95 2012 9781111578305 Straumanis Organic Chemistry p.100 29.95 2006 9789812654243 Jaafar Organic Chemistry for Matriculation p.54 39.95 2015 9781285842912 McMurry Organic Chemistry with Biological Applications, 3e p.101 351.95 2012 9781111425562 Hart Organic Chemistry, 13e p.98 265.95 2012 9781111426248 Hart Organic Chemistry, 13e p.99 265.95 2009 9780618974122 Straumanis Organic Chemistry, 2e p.95 115.95 2011 9780495391470 McMurry Organic Chemistry, 2e p.96 351.95 2014 9781285052816 Brown Organic Chemistry, International Edition, 7e p.103 229.95 2012 9780840054531 McMurry Organic Chemistry, International Edition, 8e p.105 347.95 2011 9780538733632 Williamson Organic Experiments, 6e p.106 288.95 P 2015 9781133958437 Ball Physical Chemistry, 2e p.113 289.95 2003 9780618123414 Laidler Physical Chemistry, 4e p.111 340.95 2010 9780495561293 Moore Principles of Chemistry p.54 245.95 2012 9781111427832 Oxtoby Principles of Modern Chemistry, International Edition, 7e p.56 293.95 2014 9781133951889 Weeks Pushing Electrons, 4e p.107 49.95 S 2011 9780538734547 Seager Safety-Scale Laboratory Experiments for Chemistry for Today, 7e 2014 9781133604259 Seager Safety-Scale Laboratory Experiments for Chemistry for Today, 8e p.21 129.95 p.22 129.95 2014 9781408093733 Skoog Skoog and West s Fundamentals of Analytical Chemistry, 9e p.26 260.75 2004 9780534424572 Bishop Standard and Microscale Experiments in General Chemistry, 5e 2013 9781111989408 Ebbing Study Guide for Ebbing/Gammon s General Chemistry, 10th, 10e 2015 9781285778662 Sanger Study Guide for Moore/Stanitski s Chemistry: The Molecular Science, 5th, 5e 2014 9781133933540 Whitten Study Guide for Whitten/Davis/Peck/Stanley s Chemistry, 10th, 10e p.58 176.95 p.59 112.95 p.60 121.95 p.60 127.95 Prices quoted here are correct at time of printing and are subject to change without prior notice

QTY YEAR ISBN NO. AUTHOR TITLE/EDITION PAGE NO. PRICE(USD) 2015 9781285845173 DeCoste Study Guide for Zumdahl/DeCoste s Introductory Chemistry: A Foundation, 8th, 8e p.79 97.95 2014 9781133611509 Zumdahl Study Guide for Zumdahl/Zumdahl s Chemistry, 9th, 9e p.60 112.95 2014 9781285052618 Brown Study Guide with Solutions Manual for Brown/Iverson/ Anslyn/Foote s Organic Chemistry, 7th, 7e 2015 9781305087972 McMurry Study Guide with Solutions Manual for McMurry s Organic Chemistry: With Biological Applications, 3rd, 3e 2013 9781133108511 Garrett Study Guide with Student Solutions Manual and Problems Book for Garrett/Grisham s Biochemistry, 5th, 5e 2012 9780840054456 McMurry Study Guide with Student Solutions Manual for McMurry s Organic Chemistry, 8th, 8e 2014 9781133606994 Seager Study Guide with Student Solutions Manual for Seager/ Slabaugh s Chemistry for Today, 8th, 8e 2008 9780495387510 Atwood Survival Guide for General Chemistry with Math Review, 2e p.108 189.95 p.108 136.95 p.29 133.95 p.109 196.95 p.22 121.95 p.60/p.80 51.95 2009 9780495828266 Atwood Survival Guide for Introductory Chemistry p.80 58.95 T 2012 9781111430412 Williamson Techniques Labs for Macroscale and Microscale Organic p.109 147.95 Experiments (with CourseMate 2-Semester Printed Access Card), 6e U 2011 9781111428174 Pedersen Understanding the Principles of Organic Chemistry p.110 193.95 Prices quoted here are correct at time of printing and are subject to change without prior notice

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Chemistry 2014 2015 Catalog Chemistry 2014 2015 Catalog CLA DEC 2013 Cengage Learning Asia Pte Ltd 151 Lorong Chuan #02-08 New Tech Park (Lobby H) Singapore 556741 Tel (65) 6410 1200 Fax (65) 6410 1208 e-mail asia.info@cengage.com